US12006531B2

US12006531B2 - Methods and systems for rapid detection of microorganisms using infectious agents

Info

Publication number: US12006531B2
Application number: US16/674,876
Authority: US
Inventors: Dwight Lyman Anderson; Jose S. Gil; Ben Barrett Hopkins; Stephen Erickson
Original assignee: Laboratory Corp of America Holdings
Current assignee: Laboratory Corp of America Holdings
Priority date: 2012-02-21
Filing date: 2019-11-05
Publication date: 2024-06-11
Anticipated expiration: 2033-02-21
Also published as: US20200140919A1; US20150218616A1; US10519483B2

Abstract

Disclosed herein are methods and systems for rapid detection of microorganisms in a sample, without culturing for enrichment of the microorganism. A modified bacteriophage is also disclosed which comprises a non-native indicator gene in the late gene region. The indicator product is not a fusion protein. The specificity of infectious agents allows a specific microorganism to be targeted, and an indicator signal may be amplified to optimize assay sensitivity.

Description

RELATED APPLICATIONS

The present application is a Continuation application of U.S. patent application Ser. No. 14/625,481, filed Feb. 18, 2015, which is a Continuation-in-Part application of U.S. patent application Ser. No. 13/773,339, filed Feb. 21, 2013, entitled “Methods and Systems for Detection of Microorganisms,” which claims priority under 35 USC 119(e) to U.S. Provisional Patent Application No. 61/601,231, filed Feb. 21, 2012. The present application also claims priority under 35 USC 119(e) to U.S. Provisional Patent Application No. 61/940,959, filed Feb. 18, 2014. The disclosures of U.S. Provisional Patent Application Nos. 61/601,231 and 61/940,959 and U.S. patent application Ser. Nos. 13/773,339 and 14/625,481 are incorporated by reference in their entireties herein.

FIELD OF THE INVENTION

This invention relates to methods and systems for the detection of microorganisms using infectious agents.

BACKGROUND

There is a strong interest in improving speed and sensitivity for detection of bacteria, viruses, and other microorganisms in biological, food, water, and clinical samples. Microbial pathogens can cause substantial morbidity among humans and domestic animals, as well as immense economic loss. Also, detection of microorganisms is a high priority for the Food and Drug Administration (FDA) and Centers for Disease Control (CDC) given outbreaks of life-threatening or fatal illness caused by ingestion of food contaminated with certain microorganisms, e.g., Escherichia coli or Salmonella spp.

Traditional microbiological tests for the detection of bacteria rely on non-selective and selective enrichment cultures followed by plating on selective media and further testing to confirm suspect colonies. Such procedures can require several days. A variety of rapid methods have been investigated and introduced into practice to reduce the time requirement. However, these methods have drawbacks. For example, techniques involving direct immunoassays or gene probes generally require an enrichment step in order to obtain adequate sensitivity. Polymerase chain reaction (PCR) tests also include an amplification step and therefore are capable of both very high sensitivity and selectivity; however, the sample size that can be economically subjected to PCR testing is limited. With dilute bacterial suspensions, most small subsamples will be free of cells and therefore purification and/or enrichment steps are still required.

The time required for traditional biological enrichment is dictated by the growth rate of the target bacterial population of the sample, by the effect of the sample matrix, and by the required sensitivity. For instance, a magnetic-capture PCR system for verotoxigenic E. coli can require about 5, 7 and 10 hours of culturing for enrichment to detect 1000, 100, and 1 colony forming unit per milliliter (CFU/mL), respectively, in a model system, and 15 hours of culturing for enrichment to detect 1 CFU per gram (g) in ground beef. In practice, most high sensitivity methods employ an overnight incubation and take about 24 hours overall. Due to the time required for cultivation, these methods can take up to three days, depending upon the organism to be identified and the source of the sample. This lag time is generally unsuitable as the contaminated food, water (or other product) may have already made its way into livestock or humans. In addition, increases in antibiotic-resistant bacteria and biodefense considerations make rapid identification of bacterial pathogens in water, food and clinical samples critical priorities worldwide.

Therefore, there is a need for more rapid, simple and sensitive detection and identification of microorganisms, such as bacteria, viruses, and other potentially pathogenic microorganisms.

SUMMARY

Embodiments of the invention comprise compositions, methods, systems and kits for the detection of microorganisms. The invention may be embodied in a variety of ways.

In some aspects, the invention comprises a recombinant bacteriophage comprising an indicator gene inserted into a late gene region of the bacteriophage.

In some embodiments, the invention comprises a method for detecting a microorganism of interest in a sample comprising the steps of incubating the sample with a recombinant bacteriophage that infects the microorganism of interest, wherein the recombinant bacteriophage comprises an indicator gene inserted into a late gene region of the bacteriophage such that expression of the indicator gene during bacteriophage replication following infection of host bacteria results in a soluble indicator protein product, and detecting the indicator protein product, wherein positive detection of the indicator protein product indicates that the microorganism of interest is present in the sample.

In other embodiments, the invention comprises a system for rapid detection of a microorganism of interest in a sample, comprising a component for incubating the sample with an infectious agent specific for the microorganism of interest, wherein the infectious agent comprises an indicator moiety, and a component for detecting the indicator moiety.

In still other embodiments, the invention comprises non-transient computer readable media for use with methods or systems according to the invention.

BRIEF DESCRIPTION OF THE FIGURES

The present invention may be better understood by referring to the following non-limiting figures.

FIG. 1 depicts an indicator phage construct according to an embodiment of the invention illustrating insertion of a genetic construct comprising Firefly luciferase gene and a T7 late promoter inserted into the late (class III) region of a bacteriophage. Also depicted is a sequence comprising stop codons in all three reading frames to prevent read-through and an untranslated region (UTR).

FIG. 2 shows the genome of bacteriophage JG04, a T4-like bacteriophage which was isolated from sewage treatment plant samples and shares ˜98% homology with T4-like phage RB69. Capsid proteins gp23 and gp24 are within the late gene region, consisting of structural genes, which code for virion proteins. As these virion proteins are expressed at a very high level, any genes inserted into this region can be expected to have similar expression levels, as long as late gene promoters and/or other similar control elements are used.

FIG. 3 shows three homologous recombination plasmid constructs carrying three different luciferase genes. Firefly luciferase, NANOLUC® luciferase, and Oplophorus luciferase genes are each inserted into a pUC57.Amp^Rplasmid backbone. In each construct, a fragment of the gp23 capsid protein gene is followed by a T4 late promoter, the respective luciferase gene, and a gp23-24 untranslated region. The Oplophorus construct additionally comprises a fragment of the gp24 gene downstream of the untranslated region.

FIG. 4 depicts the isolation of recombinant phage from modifications of JG04 bacteriophage using the plasmid constructs such as those shown in FIG. 3 using a series of sequential infection and dilution steps to identify recombinant phage that express an indicator gene.

FIG. 5 depicts the use of indicator phage encoding a soluble luciferase to detect bacterial cells via detection of luciferase generated from replication of progeny phage during infection of the bacterial cells, according to an embodiment of the invention

FIG. 6 demonstrates sensitivity for detection of target bacteria using indicator phage with spin columns, according to an embodiment of the invention. The approximate number of E. coli O157:H7 cells in each assay is indicated on the X-axis. The signal provided by the soluble luciferase produced upon infection of the bacteria is shown on the Y-axis as relative luminal units (RLU) over background (BG) signal (i.e., no cells) (RLU/BG).

FIG. 7 demonstrates detection of target bacteria over a range of titers using indicator phage with spin columns, according to an embodiment of the invention. The approximate number of E. coli O157:H7 cells in each assay is indicated on the X-axis. The signal provided by the soluble luciferase produced upon infection of the bacteria is shown on the Y-axis as relative luminal units (RLU) over background (BG) signal (i.e., no cells) (RLU/BG).

FIG. 8 demonstrates sensitivity for detection of target bacteria using indicator phage with 96-well filter plates, according to an embodiment of the invention. The approximate number of E. coli O157:H7 cells in each assay is indicated on the X-axis. The signal provided by the soluble luciferase produced upon infection of the bacteria is shown on the Y-axis as relative luminal units (RLU) over background (BG) signal (i.e., no cells) (RLU/BG).

FIG. 9 demonstrates detection of target bacteria over a range of titers using indicator phage with 96-well filter plates, according to an embodiment of the invention. The approximate number of E. coli O157:H7 cells in each assay is indicated on the X-axis. The signal provided by the soluble luciferase produced upon infection of the bacteria is shown on the Y-axis as relative luminal units (RLU) over background (BG) signal (i.e., no cells) (RLU/BG). The detection of luciferase activity may be continued for an extended period of time. Here, reading ⋄represents 0 time (i.e., a baseline control); Δ after 15 minutes (min); and □ after 30 minutes.

FIG. 10 depicts a filter plate assay for detecting bacteria of interest using a modified bacteriophage according to an embodiment of the invention where bacteria and recombinant phage are incubated on filter plates and after generation of progeny bacteriophage the indicator protein is detected directly without removal of the incubation medium.

FIG. 11 shows results from a filter plate assay using JG04-NANOLUC® phage to detect E. coli O157:H7 cells in samples with known cell numbers. The approximate number of E. coli O157:H7 cells in each assay is indicated on the X-axis. The signal provided by the soluble luciferase produced upon infection of the bacteria is shown on the Y-axis as relative luminal units (RLU) over background (BG) signal (i.e., no cells) (RLU/BG).

FIG. 12 depicts a “No Concentration Assay” for detecting a bacterium of interest using a modified bacteriophage according to an embodiment of the invention.

FIG. 13 shows results from a No Concentration Assay using JGO4-OpLuc phage to detect E. coli O157:H7 cells in samples with known cell numbers in the low number range. The approximate number of E. coli O157:H7 cells in each assay is indicated on the X-axis. The signal provided by the soluble luciferase produced upon infection of the bacteria is shown on the Y-axis as relative luminal units (RLU) as compared to background (X) signal (i.e., no cells).

FIG. 14 shows results from a No Concentration Assay using JG04-OpLuc phage to detect E. coli O157:H7 cells in samples with known cell numbers in the low to high number range. The approximate number of E. coli O157:H7 cells in each assay is indicated on the X-axis. The signal provided by the soluble luciferase produced upon infection of the bacteria is shown on the Y-axis as relative luminal units (RLU).

FIG. 15 shows results from a No Concentration Assay using JG04-OpLuc phage to detect E. coli O157:H7 cells in Vegetable Wash samples with known cell numbers. The approximate number of E. coli O157:H7 cells in each assay is indicated on the X-axis. The signal provided by the soluble luciferase produced upon infection of the bacteria is shown on the Y-axis as relative luminal units (RLU).

FIG. 16 demonstrates specific and quantitative capture of E. coli O157:H7 using affinity-purified, surface-specific antibodies, according to an embodiment of the invention.

FIG. 17 depicts a Hybrid Immuno-Phage (HIP) Assay for detecting a bacterium of interest using a modified bacteriophage according to an embodiment of the invention wherein antibodies to the microorganism of interest are used to capture the microorganism on the surface of the assay well prior to incubation with a recombinant infectious agent having an indicator gene.

FIG. 18 shows results from a HIP assay using JG04-NANOLUC® phage to detect E. coli O157:H7 cells in samples with known cell numbers, on a logarithmic scale. The approximate number of E. coli O157:H7 cells in each assay is indicated on the X-axis. The signal provided by the soluble luciferase produced upon infection of the bacteria is shown on the Y-axis as relative luminal units (RLU).

DETAILED DESCRIPTION OF THE INVENTION

Disclosed herein are compositions, methods and systems that demonstrate surprising sensitivity for detection of a microorganism of interest in test samples (e.g., biological, food, water, and clinical samples). Detection can be achieved in a shorter timeframe than was previously thought possible using genetically modified infectious agents in assays performed without any culturing for enrichment, or in some embodiments with minimal incubation times during which microorganisms could potentially multiply. Also surprising is the success of using high multiplicity of infection (MOI), or high concentrations of plaque forming units (PFU), for incubation with a test sample. Such high phage concentrations (PFU/mL) were previously purported to be detrimental to microorganism detection assays, as they were purported to cause “lysis from without.”

The compositions, methods, systems and kits of the invention may comprise infectious agents for use in detection of such microorganisms. In certain embodiments, the invention may comprise a composition comprising a recombinant bacteriophage having an indicator gene inserted into a late gene region of the bacteriophage. In certain embodiments, expression of the indicator gene during bacteriophage replication following infection of a host bacterium results in a soluble indicator protein product. In certain embodiments, the indicator gene may be inserted into a late gene (i.e., class III) region of the bacteriophage. The bacteriophage may be derived from T7, T4, JG04, or another natural bacteriophage.

In some aspects, the invention comprises a method for detecting a microorganism of interest. The method may use an infectious agent for detection of the microorganism of interest. For example, in certain embodiments, the microorganism of interest is a bacterium and the infectious agent is a bacteriophage. Thus, in certain embodiments, the method may comprise detection of a microorganism of interest in a sample by incubating the sample with a recombinant bacteriophage that infects the microorganism of interest. In certain embodiments, the recombinant bacteriophage comprises an indicator gene. The indicator gene may, in certain embodiments, be inserted into a late gene region of the bacteriophage such that expression of the indicator gene during bacteriophage replication following infection of host bacteria results in a soluble indicator protein product. The method may comprise detecting the indicator protein product, wherein positive detection of the indicator protein product indicates that the microorganism of interest is present in the sample.

In certain embodiments, the invention may comprise a system. The system may contain at least some of the compositions of the invention. Also, the system may comprise at least some of the components for performing the method. In certain embodiments, the system is formulated as a kit. Thus, in certain embodiments, the invention may comprise a system for rapid detection of a microorganism of interest in a sample, comprising: a component for incubating the sample with an infectious agent specific for the microorganism of interest, wherein the infectious agent comprises an indicator moiety; and a component for detecting the indicator moiety. In yet other embodiments, the invention comprises software for use with the methods or systems.

Thus, some embodiments of the present invention solve a need by using infectious agent-based methods for amplifying a detectable signal indicating the presence of bacteria. In certain embodiments as little as a single bacterium is detected. The principles applied herein can be applied to the detection of a variety of microorganisms. Because of numerous binding sites for an infectious agent on the surface of a microorganism, the capacity to produce one hundred or more agent progeny during infection, and the potential for high level expression of an encoded indicator moiety, the infectious agent or an indicator moiety can be more readily detectable than the microorganism itself. In this way, embodiments of the present invention can achieve tremendous signal amplification from even a single infected cell.

Aspects of the present invention utilize the high specificity of binding agents that can bind to particular microorganisms, such as the binding component of infectious agents, as a means to detect and/or quantify the specific microorganism in a sample. In some embodiments, the present invention utilizes the high specificity of infectious agents such as bacteriophage.

In some embodiments, detection is achieved through an indicator moiety associated with the binding agent specific for the microorganism of interest. For example, an infectious agent may comprise an indicator moiety. In some embodiments the indicator may be encoded by the infectious agent, such as a bacteriophage, and the bacteriophage is designated an indicator phage.

Some embodiments of the invention disclosed and described herein utilize the discovery that a single microorganism is capable of binding specific recognition agents, such as phage. Following infection and replication of the phage, progeny phage may be detected via an indicator moiety expressed during phage replication. This principle allows amplification of indicator signal from one or a few cells based on specific recognition of microorganism surface receptors. For example, by exposing even a single cell of a microorganism to a plurality of phage, thereafter allowing amplification of the phage and high-level expression of an encoded indicator gene product during replication, the indicator signal is amplified such that the single microorganism is detectable.

Embodiments of the methods and systems of the invention can be applied to detection and quantification of a variety of microorganisms (e.g., bacteria, fungi, yeast) in a variety of circumstances, including but not limited to detection of pathogens from food, water, clinical and commercial samples. The methods of the present invention provide high detection sensitivity and specificity rapidly and without the need for traditional biological enrichment (e.g., culturing for enrichment), which is a surprising aspect as all available methods require culturing. In some embodiments detection is possible within 1-2 replication cycles of the bacteriophage or virus, which goes against conventional wisdom, as it doesn't take advantage of the phage's natural ability to amplify itself and the luciferase signal.

Definitions

Unless otherwise defined herein, scientific and technical terms used in connection with the present invention shall have the meanings that are commonly understood by those of ordinary skill in the art. Further, unless otherwise required by context, singular terms shall include pluralities and plural terms shall include the singular. Generally, nomenclatures used in connection with, and techniques of, cell and tissue culture, molecular biology, immunology, microbiology, genetics and protein and nucleic acid chemistry and hybridization described herein are those well known and commonly used in the art. Known methods and techniques are generally performed according to conventional methods well known in the art and as described in various general and more specific references that are discussed throughout the present specification unless otherwise indicated. Enzymatic reactions and purification techniques are performed according to manufacturer's specifications, as commonly accomplished in the art or as described herein. The nomenclatures used in connection with the laboratory procedures and techniques described herein are those well-known and commonly used in the art.

The following terms, unless otherwise indicated, shall be understood to have the following meanings:

As used herein, the terms “a”, “an”, and “the” can refer to one or more unless specifically noted otherwise.

The use of the term “or” is used to mean “and/or” unless explicitly indicated to refer to alternatives only or the alternatives are mutually exclusive, although the disclosure supports a definition that refers to only alternatives and “and/or.” As used herein “another” can mean at least a second or more.

Throughout this application, the term “about” is used to indicate that a value includes the inherent variation of error for the device, the method being employed to determine the value, or the variation that exists among samples.

The term “solid support” or “support” means a structure that provides a substrate and/or surface onto which biomolecules may be bound. For example, a solid support may be an assay well (i.e., such as a microtiter plate or multi-well plate), or the solid support may be a location on a filter, an array, or a mobile support, such as a bead or a membrane (e.g., a filter plate or lateral flow strip).

The term “antibody” includes monoclonal antibodies, polyclonal antibodies, synthetic antibodies and chimeric antibodies, e.g., generated by combinatorial mutagenesis and phage display. The term “antibody” also includes mimetics or peptidomimetics of antibodies. Peptidomimetics are compounds based on, or derived from, peptides and proteins. The peptidomimetics of the present invention typically can be obtained by structural modification of a known peptide sequence using unnatural amino acids, conformational restraints, isosteric replacement, and the like. Fragments of antibodies may serve in place of antibodies in some embodiments. “Surface-specific antibodies” as used herein bind to molecules exposed on the outer surface of a specific microorganism.

As used herein, the term “free antibodies” refers to antibodies which are in solution and may move freely through a liquid; i.e., they are not initially bound to a solid support or otherwise constrained.

As used herein, “affinity-purified” or “affinity-purification” refers to a series of steps used to prepare and treat antibodies such that they exhibit optimal specificity and sensitivity, including minimal cross-reactivity with undesired epitopes. For example, removal of undesired lipids and proteins from antiserum may first be achieved by salt precipitation steps. Further positive selection (also called “affinity-purification”) and/or negative selection (also called “reverse-purification”) may be achieved by passing the remaining antibodies over a support (e.g., agarose columns) comprising surface antigens designed to retain antibodies with particular epitope affinities. In some examples, where the starting antiserum is polyclonal, the purified antibodies that remain after these selection steps are able to recognize many different epitopes on the surface of the microorganism of interest, but they do not recognize the surface epitopes of other microorganisms.

The term “binding agent” refers to a molecule that can specifically and selectively bind to a second (i.e., different) molecule of interest. The interaction may be non-covalent, for example, as a result of hydrogen-bonding, van der Waals interactions, or electrostatic or hydrophobic interactions, or it may be covalent. The term “soluble binding agent” refers to a binding agent that is not associated with (i.e., covalently or non-covalently bound) to a solid support.

As used herein, an “analyte” refers to a molecule, compound or cell that is being measured. The analyte of interest may, in certain embodiments, interact with a binding agent. As described herein, the term “analyte” may refer to a protein or peptide of interest. An analyte may be an agonist, an antagonist, or a modulator. Or, an analyte may not have a biological effect. Analytes may include small molecules, sugars, oligosaccharides, lipids, peptides, peptidomimetics, organic compounds and the like.

The term “detectable moiety” or “detectable biomolecule” or “reporter” or “indicator moiety” refers to a molecule that can be measured in a quantitative assay. For example, an indicator moiety may comprise an enzyme that may be used to convert a substrate to a product that can be measured. An indicator moiety may be an enzyme that catalyzes a reaction that generates bioluminescent emissions (e.g., luciferase). Or, an indicator moiety may be a radioisotope that can be quantified. Or, an indicator moiety may be a fluorophore. Or, other detectable molecules may be used.

As used herein, “bacteriophage” or “phage” includes one or more of a plurality of bacterial viruses. In this disclosure, the terms “bacteriophage” and “phage” include viruses such as mycobacteriophage (such as for TB and paraTB), mycophage (such as for fungi), mycoplasma phage, and any other term that refers to a virus that can invade living bacteria, fungi, mycoplasma, protozoa, yeasts, and other microscopic living organisms and uses them to replicate itself. Here, “microscopic” means that the largest dimension is one millimeter or less. Bacteriophages are viruses that have evolved in nature to use bacteria as a means of replicating themselves. A phage does this by attaching itself to a bacterium and injecting its DNA (or RNA) into that bacterium, and inducing it to replicate the phage hundreds or even thousands of times. This is referred to as phage amplification.

As used herein, “late gene region” refers to a region of a viral genome that is transcribed late in the viral life cycle. The late gene region typically includes the most abundantly expressed genes (e.g., structural proteins assembled into the bacteriophage particle). Late genes are synonymous with class III genes and include genes with structure and assembly functions. For example, the late genes (synonymous with class III,) are transcribed in T7, e.g., from 8 minutes after infection until lysis, class I (e.g., RNA polymerase) is early from 4-8 minutes, and class II from 6-15 minutes, so there is overlap in timing of II and III. A late promoter is one that is naturally located and active in such a late gene region.

As used herein, “culturing for enrichment” refers to traditional culturing, such as incubation in media favorable to propagation of microorganisms, and should not be confused with other possible uses of the word “enrichment,” such as enrichment by removing the liquid component of a sample to concentrate the microorganism contained therein, or other forms of enrichment that do not include traditional facilitation of microorganism propagation. Culturing for enrichment for very short periods of time may be employed in some embodiments of methods described herein, but is not necessary and is for a much shorter period of time than traditional culturing for enrichment, if it is used at all.

As used herein “recombinant” refers to genetic (i.e., nucleic acid) modifications as usually performed in a laboratory to bring together genetic material that would not otherwise be found. This term is used interchangeably with the term “modified” herein.

Samples

Each of the embodiments of the methods and systems of the invention can allow for the rapid detection and quantification of microbes in a sample. For example, methods according to the present invention can be performed, most preferably, in about two hours or less.

Microbes detected by the methods and systems of the present invention include pathogens that are of commercial, medical or veterinary concern. Such pathogens include Gram-negative bacteria, Gram-positive bacteria, mycoplasmas and viruses. Any microbe for which an infectious agent that is specific for the particular microbe has been identified can be detected by the methods of the present invention. Those skilled in the art will appreciate that there is no limit to the application of the present methods other than the availability of the necessary specific infectious agent/microbe pairs.

Bacterial cells detectable by the present invention include, but are not limited to, bacterial cells that are food or water borne pathogens. Bacterial cells detectable by the present invention include, but are not limited to, all species of Salmonella, all strains of Escherichia coli, including, but not limited to E. coli O157:H7, all species of Listeria, including, but not limited to L. monocytogenes, and all species of Campylobacter. Bacterial cells detectable by the present invention include, but are not limited to, bacterial cells that are pathogens of medical or veterinary significance. Such pathogens include, but are not limited to, Bacillus spp., Bordetella pertussis, Camplyobacter jejuni, Chlamydia pneumoniae, Clostridium perfringens, Enterobacter spp., Klebsiella pneumoniae, Mycoplasma pneumoniae, Salmonella typhi, Shigella sonnei, Staphylococcus aureus, and Streptococcus spp.

The sample may be environmental or food or water samples and medical or veterinary samples. Samples may be liquid, solid, or semi-solid. Samples may be swabs of solid surfaces. Samples may include environmental materials, such as the water samples, or the filters from air samples or aerosol samples from cyclone collectors. Samples may be of meat, poultry, processed foods, milk, cheese, or other dairy products. Medical or veterinary samples include, but are not limited to, blood, sputum, cerebrospinal fluid, and fecal samples and different types of swabs.

Samples may be used directly in the detection methods of the present invention, without preparation, concentration, or dilution. For example, liquid samples, including but not limited to, milk and juices, may be assayed directly. Samples may be diluted or suspended in solution, which may include, but is not limited to, a buffered solution or a bacterial culture medium. A sample that is a solid or semi-solid may be suspending in a liquid by mincing, mixing or macerating the solid in the liquid. A sample should be maintained within a pH range that promotes bacteriophage attachment to the host bacterial cell. A sample should also contain the appropriate concentrations of divalent and monovalent cations, including but not limited to Na⁺, Mg²⁺, and K⁺. Preferably a sample is maintained at a temperature that maintains the viability of any pathogen cells contained within the sample.

Preferably throughout detection assays, the sample is maintained at a temperature that maintains the viability of any pathogen cell present in the sample. During steps in which bacteriophages are attaching to bacterial cells, it is preferable to maintain the sample at a temperature that facilitates bacteriophage attachment. During steps in which bacteriophages are replicating within an infected bacterial cell or lysing such an infected cell, it is preferable to maintain the sample at a temperature that promotes bacteriophage replication and lysis of the host. Such temperatures are at least about 25 degrees Celsius (C), more preferably no greater than about 45 degrees C., most preferably about 37 degrees C. It is also preferred that the samples be subjected to gentle mixing or shaking during bacteriophage attachment, replication and cell lysis.

Assays may include various appropriate control samples. For example, control samples containing no bacteriophages or control samples containing bacteriophages without bacteria may be assayed as controls for background signal levels.

Indicator Infectious Agents

As described in more detail herein, the compositions, methods, systems and kits of the invention may comprise infectious agents for use in detection of such microorganisms. In certain embodiments, the invention may comprise a composition comprising a recombinant bacteriophage having an indicator gene inserted into a late gene region of the bacteriophage. As described in more detail below, in certain embodiments of the infectious agent, the indicator gene does not encode a fusion protein. For example, in certain embodiments, expression of the indicator gene during bacteriophage replication following infection of a host bacterium results in a soluble indicator protein product. In certain embodiments, the indicator gene may be inserted into a late gene region of the bacteriophage. In a recombinant bacteriophage the late gene region may be a class III gene region.

In some embodiments, the indicator phage is derived from T7, T4 or another phage. An indicator bacteriophage may also be derived from T7-like, T4-like, JG04, JG04-like, or any other bacteriophage having a genome with at least 99, 98, 97, 96, 95, 94, 93, 92, 91 90, 89, 88, 87, 86, 85, 84, 83, 82, 81, 80, 79, 78, 77, 76, 75, 74, 73, 72, 71, or 70% homology to T7, T7-like, T4, T4-like, JG04, or JG04-like phages. In some embodiments, the indicator phage is derived from a natural phage isolated from the environment, such as JG04 phage, a T4-like phage isolated as described in the Examples. The genetic modifications may avoid deletions of wild-type genes and thus remain more similar to the wild-type infectious agent than many commercially available phage, e.g. T7SELECT®415. Such naturally derived bacteriophage may be more specific for bacteria that are found in the environment than bacteriophage that are commercially available and as such, genetically distinct from phage found in the environment.

Moreover, phage genes thought to be nonessential may have unrecognized function. For example, an apparently nonessential gene may have an important function in elevating burst size with subtle cutting, fitting, or trimming functions in assembly. As such, deleting genes to insert an indicator may be detrimental. Most phages can package a DNA that is a few percent larger than their natural genome. With this consideration, a smaller indicator gene may be a more appropriate choice for modifying a bacteriophage, especially one with a smaller genome. OpLuc and NANOLUC® proteins are only about 20 kDa (approximately 500-600 bp to encode), while FLuc is about 62 kDa (approximately 1,700 bp to encode). For comparison, the genome of T7 is around 40 kbp, while the T4 genome is about 170 kbp.

In some indicator phage embodiments, the indicator gene may be inserted into an untranslated region to avoid disruption of functional genes, leaving wild-type phage genes intact, which may lead to greater fitness when infecting non-laboratory strain bacteria. Additionally, stop codons at all three reading frames may help to increase expression by reducing read-through, also known as leaky expression. This strategy may also eliminate the possibility of a fusion protein being made at low levels, which would manifest as background signal (e.g., luciferase) that cannot be separated from the phage.

An indicator gene may express a variety of biomolecules. The indicator gene is a gene that expresses a detectable product or an enzyme that produces a detectable product. For example, in one embodiment the indicator gene encodes a luciferase enzyme. Various type of luciferase may be used. In alternate embodiments, and as described in more detail herein, the luciferase is one of Oplophorus luciferase, Firefly luciferase, or an engineered luciferase.

Thus, in some embodiments, the present invention comprises a modified bacteriophage comprising a non-bacteriophage indicator gene in the late (class III) gene region. In some embodiments, the non-native indicator gene is under the control of a late promoter. Using a viral late gene promoter insures the reporter gene (luciferase) is not only expressed at high levels, like viral capsid proteins, but also does not shut down like endogenous bacterial genes or even early viral genes.

In some embodiments, the late promoter is a T4- or T7-like promoter, or another phage promoter similar to that found in the natural phage without genetic modification. The late gene region may be a class III gene region, and the bacteriophage may be derived from T7, T4, T4-like, JG04, or another natural bacteriophage having a genome with at least 90% homology to T7, T4 or T4-like phages. In preferred embodiments, the indicator gene does not encode a fusion protein.

Genetic modifications to infectious agents may include insertions, deletions, or substitutions of a small fragment of nucleic acid, a substantial part of a gene, or an entire gene. In some embodiments, inserted or substituted nucleic acids comprise non-native sequences. A non-native indicator gene may be inserted into a bacteriophage genome such that it is under the control of a bacteriophage promoter. In some embodiments, the non-native indicator gene is not part of a fusion protein. That is, in some embodiments, a genetic modification may be configured such that the indicator protein product does not comprise polypeptides of the natural bacteriophage. In some embodiments, the indicator protein product is soluble. In some embodiments, the invention comprises a method for detecting a microorganism of interest comprising the step of incubating a test sample with such a modified bacteriophage.

In some embodiments, the non-native indicator gene is not contiguous with a gene encoding a structural phage protein and therefore does not yield a fusion protein. In some embodiments, expression of the indicator gene in progeny bacteriophage following infection of host bacteria results in a soluble protein product.

Unlike systems which employ a fusion of a detection moiety to the capsid protein (i.e., a fusion protein), some embodiments of the present invention express a soluble luciferase. This may greatly increase the sensitivity of the assay (down to a single bacterium), and simplifies the assay, allowing the assay to be completed in less than an hour for some embodiments, as opposed to several hours due to additional purification steps required with constructs that produce detectable fusion proteins. Further, fusion proteins may be less active than soluble proteins due, e.g., to protein folding constraints that may alter the conformation of the enzyme active site or access to the substrate.

Furthermore, fusion proteins by definition limit the number of the moieties attached to subunits of a protein in the bacteriophage. For example, using a commercially available system designed to serve as a platform for a fusion protein would result in about 415 copies of the fusion moiety, corresponding to the about 415 copies of the gene 10B capsid protein in each T7 bacteriophage particle. Without this constraint, infected bacteria can be expected to express many more copies of the detection moiety (e.g., luciferase) than can fit on the bacteriophage. Additionally, large fusion proteins, such as a capsid-luciferase fusion, may inhibit assembly of the bacteriophage particle, thus yielding fewer bacteriophage progeny. Thus a soluble, non-fusion indicator gene product may be preferable.

In some embodiments, the indicator phage encodes a detectable enzyme. The indicator may emit light and/or may be detectable by a color change. Various appropriate enzymes are commercially available, such as alkaline phosphatase (AP), horseradish peroxidase (HRP), or luciferase (Luc). In some embodiments, these enzymes may serve as the indicator moiety. In some embodiments, Firefly luciferase is the indicator moiety. In some embodiments, Oplophorus luciferase is the indicator moiety. In some embodiments, NANOLUC® is the indicator moiety. Other engineered luciferases or other enzymes that generate detectable signals may also be appropriate indicator moieties.

Also, the use of a soluble detection moiety eliminates the need to isolate contaminating parental phage from the lysate of the infected sample cells. With a fusion protein system, any bacteriophage used to infect sample cells would have the detection moiety attached, and would be indistinguishable from the daughter bacteriophage also containing the detection moiety. As detection of sample bacteria relies on the detection of newly created (de novo synthesized) detection moiety, using fusion constructs requires additional steps to separate old (parental) moieties from newly created (daughter bacteriophage) moieties. This may be accomplished by washing the infected cells multiple times, prior to the completion of the bacteriophage life cycle, inactivating excess parental phage after infection by physical or chemical means, and/or chemically modifying the parental bacteriophage with a binding moiety (such as biotin), which can then be bound and separated (such as by streptavidin-coated sepharose beads). However, even with all these attempts at isolation, parental phage typically remain when a high multiplicity of infection (MOI) is used to assure infection of a low number of sample cells, creating background signal that may obscure detection of signal from infected cell progeny phage.

By contrast, with the soluble detection moiety expressed in some embodiments of the present invention, purification of the parental phage from the final lysate is unnecessary, as the parental phage will not have any detection moiety attached. Thus any detection moiety present after infection must have been created de novo, indicating the presence of an infected bacterium or bacteria. To take advantage of this benefit, the production and preparation of parental phage may include purification of the phage from any free detection moiety produced during the production of parental bacteriophage in bacterial culture. Standard bacteriophage purification techniques may be employed to purify some embodiments of phage according to the present invention, such as sucrose density gradient centrifugation, cesium chloride isopycnic density gradient centrifugation, HPLC, size exclusion chromatography, and dialysis or derived technologies (such as Amicon brand concentrators—Millipore, Inc.). The Examples herein describe the use cesium chloride isopycnic ultracentrifugation as part of the preparation of recombinant phage of the invention so as to separate parental phage particles from contaminating luciferase protein produced upon propagation of the phage in the bacteria stock. In this way, the recombinant bacteriophage of the invention is substantially free of any luciferase generated during production of the bacteria. Removal of residual luciferase present in the phage stock can substantially reduce background signal seen when the recombinant bacteriophage are incubated with a test sample.

In some embodiments of modified bacteriophage, the late promoter (class III promoter, e.g., from T7 or T4) has high affinity for RNA polymerase of the same native bacteriophage (e.g., T7 or T4, respectively) that transcribes genes for structural proteins assembled into the bacteriophage particle. These proteins are the most abundant proteins made by the phage, as each bacteriophage particle comprises dozens or hundreds of copies of these molecules. The use of a viral late promoter can ensure optimally high level of expression of the luciferase detection moiety. The use of a late viral promoter derived from, specific to, or active under the original wild-type bacteriophage the Indicator Phage is derived from (e.g., the T4 or T7 late promoter with a T4- or T7-based system) can further ensure optimal expression of the detection moiety. The use of a standard bacterial (non-viral/non-bacteriophage) promoter may in some cases be detrimental to expression, as these promoters are often down-regulated during bacteriophage infection (in order for the bacteriophage to prioritize the bacterial resources for phage protein production). Thus, in some embodiments, the phage is preferably engineered to encode and express at high level a soluble (free) indicator moiety, which does not limit expression to the number of subunits of a phage structural component.

Embodiments employing modified bacteriophage of the invention may allow rapid detection of specific bacterial strains, with total assay times as fast as 45 minutes-1.5 hours. The amount of time required may be somewhat shorter or longer depending on the strain of bacteriophage and the strain of bacteria to be detected in the assay.

The strategy of using indicator phage that produce soluble luciferase employs phage (e.g., T4 phage) engineered to express a soluble luciferase during replication instead of a capsid protein-luciferase fusion. Expression of luciferase is driven by a viral capsid promoter (e.g., the Soc promoter in T4 bacteriophage), yielding high expression. Parental phage will be free of luciferase, so any luciferase detected in the assay must come from replication of progeny phage released from the bacterial cells. Thus, there is no need to separate out the parental phage and the progeny phage.

In some embodiments, at least part of the sample comprising the bacteria to be quantified is spin filtered to remove the media and an appropriate multiplicity of biotinylated T4 phage that express luciferase are added. The parental and progeny phage in the filtrate from the infected bacteria may then be collected, e.g., by centrifugation and the level of luciferase quantified using a luminometer.

FIG. 1 depicts a schematic representation of the genomic structure of a recombinant bacteriophage of the invention, Indicator Phage T7SELECT®415-Luc. For the embodiment depicted in FIG. 1 , the detection moiety is encoded by a Firefly luciferase gene 100 inserted within the late (class III) gene region 110, which is expressed late in the viral life cycle. Late genes are generally expressed at higher levels than other phage genes, as they code for structural proteins. Thus, in the embodiment of the recombinant phage depicted by FIG. 1 , the indicator gene (i.e., Firefly luciferase) is inserted into the late gene region, just after gene 10B (major capsid protein), and is a construct comprising the Firefly luciferase gene 100. The construct depicted in FIG. 1 was designed to include stop codons 120 in all 3 reading frames to ensure luciferase is not incorporated into the gene 10B product. Also as depicted by FIG. 1 , the construct may comprise the consensus T7 late promoter 130 to drive transcription and expression of the luciferase gene. The construct may also comprise a composite untranslated region synthesized from several T7 UTRs 140. This construct ensures soluble Firefly luciferase is produced such that expression is not limited to the number of capsid proteins inherent in the phage display system.

As noted herein, in certain embodiments, it may be preferred to utilize infectious agents that have been isolated from the environment for production of the infectious agents of the invention. In this way, infectious agents that are specific to naturally derived microorganisms may be generated.

For example, FIG. 2 shows the genome of bacteriophage JG04, a natural phage having about 98% sequence homology to a T4-like bacteriophage, RB69. Isolation of the JG04 bacteriophage from a sewage treatment plant sample is described with particularity in the Examples herein. As discussed in the Examples, the capsid proteins, gp23 (220) and gp24 (230) are within the late gene region (210), consisting of structural genes, which code for virion proteins. As these virion proteins are expressed at a very high level, any genes inserted into this region can be expected to have similar expression levels, as long as late gene promoters and/or other similar control elements are used. The bacteriophage construct depicted in FIG. 2 has the sequence as set forth in SEQ ID NO: 3.

The compositions of the invention may comprise various infectious agents and/or indicator genes. For example, FIG. 3 shows three homologous recombination plasmid constructs carrying three different luciferase genes. Three constructs were made and used in recombination with JG04 to generate recombinant bacteriophage of the invention. Thus, the top construct in FIG. 3 shows a recombination plasmid having Firefly luciferase construct used for homologous recombination insertion of the Firefly luciferase into JG04: homologous recombination plasmid pUC57.HR.Fluc, corresponding to SEQ ID NO. 5. The middle construct in FIG. 3 shows a recombination plasmid used for homologous recombination insertion of the NANOLUC® luciferase into JG04: homologous recombination plasmid pUC57.HR.NANOLUC® corresponding to SEQ ID NO. 6; and the lower construct in FIG. 3 shows a recombination plasmid used for homologous recombination insertion of the Oplophorus luciferase into JG04: homologous recombination plasmid pUC19.HR.OpLuc.KanR, corresponding to SEQ ID NO. 7.

In some embodiments, indicator phage according to the invention comprise JG04 genetically engineered to comprise any one of the three constructs shown in FIG. 3 . That is, an indicator phage comprising the sequence of SEQ ID NO. 3, further comprising additional sequence inserted between nucleotides 116,555 and 119,830 of SEQ ID NO. 3 corresponding to nucleotides 402-2,973 of SEQ ID NO. 5 (or a portion thereof); or nucleotides 402-1,922 of SEQ ID NO. 6 (or a portion thereof), also called JG04-NANOLUC® Indicator Phage in Examples 6 and 11 herein; or nucleotides 2,241-4,729 of SEQ ID NO. 7 (or a portion thereof), also called JG04-OpLuc Indicator Phage in Examples 7-9 herein. For example, a portion thereof may comprise the luciferase portion only (i.e., nucleotides 943-2,595 of SEQ ID NO. 5; or nucleotides 943-1,542 of SEQ ID NO. 6; or nucleotides 2,784-3,296 of SEQ ID NO. 7). A portion thereof may further comprise the T4 late promoter (i.e., nucleotides 908-936 of either SEQ ID NO. 5 or NO. 6, or nucleotides 2,749-2,777 of SEQ ID NO. 7). In other embodiments, such indicator phage are comprised in systems or kits according to the invention. Methods described herein may also utilize such indicator phage.

FIG. 4 depicts the isolation of recombinant phage from modifications of JG04 bacteriophage using the plasmid constructs shown in FIG. 3 and described in Example 6.

In the first step 402, bacteria transformed with homologous recombination plasmid are infected with bacteriophage, resulting in progeny phage with a mixture of parental and recombinant phage with a ratio of approximately 20,000 wild-type 432:1 recombinant phage 434. The resulting recombinant phage mix is diluted 404 into 96-well plates 406 to give an average of 3 recombinant transducing units (TU) per plate, which corresponds to about 625 infectious units (IU) of mostly wild-type phage per well. The 96-well plate is assayed for luciferase activity to identify wells 436 containing recombinant phage as compared to wells 440 containing wild-type bacteriophage. Bacteria 438 are added 408; for example, each well may contain about 50 μL of turbid E. coli O157:H7. This allows the phage to replicate and produce the luciferase enzyme 442. After 2 hours of incubation at 37° C. shown in 410, wells may be screened for the presence of luciferase 442. Any positive wells are likely to have been inoculated with a single recombinant phage, and at this stage the mixture may contain a ratio of approximately 600 wild-type phage:1 recombinant, an enrichment over the original 20,000:1 ratio. In one embodiment, soluble luciferase and phage were present at approximate ratio of 625 wild-type:1 recombinant. Progeny from this enriched culture 412 may be subjected to additional limiting dilution assay(s) 414 to verify the ratio and determine the actual concentration of recombinant phage transducing units. For example, about 3 recombinant TU per 96-well plate 416 may be aliquoted 414 from the first purification stock, leading to an approximate inoculation of ˜20 mostly wild-type phage per well of a second dilution assay plate 420. Any positive luciferase wells are likely to have been inoculated with a single recombinant along with ˜20 wild-type phage. These wells may be analyzed for presence of luciferase 442.

After addition of bacteria and incubation (e.g., 37° C. for 2 hours) 418, soluble luciferase and phage are present at approximately 20 wild-type: 1 recombinant 420. Finally, a plaque assay may be performed 422 to screen for recombinants that express luciferase 446. A small number of individual (e.g., n=48) plaques may be individually picked and screened on a third multiwell plate 426 for luciferase activity 436. In an embodiment, this approach should insure that about 3 recombinants would be in the mix of plaques being screened. One plaque may be removed from the plate to each well of a 96-well plate 424 and a luciferase assay performed 426 to determine which wells contained phage exhibiting luciferase activity 442. Wells 428 demonstrating luciferase activity represent pure recombinant phage 434, while wells without luciferase activity 430 represent pure wild-type phage 432.

Individual plaques may then be suspended in buffer or media (e.g., 100 μL TMS), and an aliquot (e.g., about 5 μL) added to a well containing a turbid E. coli O157:H7 culture, and assayed after incubation (e.g., about 45 minutes to 1 hour at 37° C.). Positive wells are expected to contain a pure culture of recombinant phage. Still, it may be preferred, in certain embodiments to include an additional round of plaque purification.

Thus, as exemplified by FIG. 4 , recombinant phage generated by homologous recombination of the appropriate recombination plasmid with JG04 can be isolated from a mixture comprising 0.005% of total phage. Following isolation, large scale production may be performed to obtain high titer stocks appropriate for use in the E. coli O157:H7 detection assay. For example, as described in more detail in the Examples herein, cesium chloride isopycnic density gradient centrifugation may be used to separate phage particles from contaminating luciferase protein to reduce background.

In this way, and as described in more detail in the Examples below, recombinant bacteriophage having the luciferase gene of interest (e.g., Firefly, Oplophorus or an engineered luciferase such as NANOLUC®) inserted into a bacteriophage derived from the environment may be generated.

Methods of Using Infectious Agents for Detecting Microorganisms

As noted herein, in certain embodiments, the invention may comprise methods of using infectious particles for detecting microorganisms. The methods of the invention may be embodied in a variety of ways.

Thus, the methods of the present invention utilizes the high specificity of binding agents that recognize and bind to a particular microorganism of interest as a means to amplify a signal and thereby detect low levels of a microorganism (e.g., a single microorganism) present in a sample. For example, infectious agents (e.g., bacteriophage) specifically recognize surface receptors of particular microorganisms and thus specifically infect those microorganisms. As such, these infectious agents may be appropriate binding agents for targeting a microorganism of interest. Some embodiments of the invention utilize the specificity of binding and high-level genetic expression capacity of infectious agents for rapid and sensitive targeting to infect and facilitate detection of a microorganism of interest.

Thus, in an embodiment, the invention may comprise a method for detecting a microorganism of interest in a sample comprising the steps of: incubating the sample with an infectious agent that infects the microorganism of interest, wherein the infectious agent comprises an indicator gene such that expression of the indicator gene during bacteriophage replication following infection of microorganism of interest results in a soluble indicator protein product; and detecting the indicator protein product, wherein positive detection of the indicator protein product indicates that the microorganism of interest is present in the sample.

A variety of infectious agents may be used. In alternate embodiments, bacteriophages, phages, mycobacteriophages (such as for TB and paraTB), mycophages (such as for fungi), mycoplasma phages, and any other virus that can invade living bacteria, fungi, mycoplasma, protozoa, yeasts, and other microscopic living organisms can be employed to target a microorganism of interest. For example, in an embodiment, where the microorganism of interest is a bacterium, the infectious agent may comprise a bacteriophage. As discussed herein, such bacteriophage may replicate inside of the bacteria to generate hundreds of progeny bacteria. Detection of the indicator gene inserted into the bacteriophage can be used as a measure of the bacteria in the sample. For example, well-studied phages of E. coli include T1, T2, T3, T4, T5, T7, and lambda; other E. coli phages available in the ATCC collection, for example, include phiX174, S13, Ox6, MS2, phiV1, fd, PR772, and ZIK1. Alternatively, natural bacteriophage may be isolated from a variety of environmental sources. A source for phage isolation may be selected based on the location where a microorganism of interest is expected to be found. Thus, in some embodiments, the indicator bacteriophage comprises an indicator moiety and infection of a single E. coli cell may be detected in an amplified signal generated via the indicator moiety. Thus the method may comprise detecting an indicator moiety produced during phage replication, wherein detection of the indicator indicates that the bacterium of interest is present in the sample.

In an embodiment, the invention may comprise a method for detecting a bacteria of interest in a sample comprising the steps of: incubating the sample with a recombinant bacteriophage that infects the bacteria of interest, wherein the recombinant bacteriophage comprises an indicator gene inserted into a late gene region of the bacteriophage such that expression of the indicator gene during bacteriophage replication following infection of host bacteria results in a soluble indicator protein product; and detecting the indicator protein product, wherein positive detection of the indicator protein product indicates that the bacteria of interest is present in the sample. In an embodiment, and as described in detail herein, the amount of indicator moiety detected corresponds to the amount of the bacteria of interest present in the sample.

In an embodiment, the late gene region is a class III gene region. As described in more detail herein, insertion of the indicator gene into the late class III gene region may ensure that the indicator gene is expressed in high quantities upon replication in the bacterium.

As described above for the compositions of the invention, the bacteriophage is derived from T7, T4, T4-like, JG04, or another natural bacteriophage having a genome with at least 90% homology to T7, T4 or other T4-like phage.

Also, in certain embodiments, the indicator gene does not encode a fusion protein. Thus, in certain embodiments, expression of the indicator gene during bacteriophage replication following infection of host bacteria results in a soluble indicator protein product.

A variety of indicator moieties may be used. In certain embodiments, the indicator gene may encode a luciferase enzyme. For example, the luciferase may be one of Oplophorus luciferase, Firefly luciferase, or an engineered luciferase.

As described in more detail herein, the methods and systems of the invention may utilize a variety of multiplicities of infection (MOI). In certain embodiments, the MOI is higher that standard assays. Such a relatively high MOI may allow for infection of microorganisms that are present at very low amounts in the sample. For example, in certain embodiments, the bacteriophage concentration for the incubating step is greater than 1×10⁷PFU/mL.

In certain embodiments, the recombinant infectious agent may be purified so as to be free of any residual indicator protein that may be generated upon production of the infectious agent stock. Thus, in certain embodiments, and as described in more detail herein, the recombinant bacteriophage may be purified using cesium chloride isopycnic density gradient centrifugation prior to incubation with the sample. When the infectious agent is a bacteriophage, this purification may have the added benefit of removing bacteriophage that do not have DNA (i.e., empty phage).

As described further below, in certain embodiments, the method may employ a step whereby the microorganism of interest is concentrated or captured from a large volume of sample. Thus, in certain embodiments, the method may comprise a step for capturing the microorganism from the sample on a solid support before the incubating step.

In some embodiments, the method may include contacting a microorganism captured on a solid support (e.g., a magnetic bead or a filter substrate) with a plurality of the specific infectious agent (e.g., indicator bacteriophage) and allowing the bacteriophage to bind and infect the bacteria. In other embodiments, capture of the microorganism is not necessary for detection. A variety of solid supports may be used. In certain embodiments, the solid support may comprise a multi-well plate, a filter, a bead, or a lateral flow strip, a filter strip, filter disc, or filter paper, or thin films designed for culturing cells (e.g., PetriFilm by 3M). Other solid supports may also be appropriate.

The microorganism of interest may be purified from the sample by using a binding agent. For example, in certain embodiments, the capturing step further comprises binding microorganism with a capture antibody. The antibody may be used in conjunction with the solid support. For example, in certain embodiments, the capture antibody facilitates binding of the microorganism to the solid support.

The method of the invention may comprise various steps to increase sensitivity. For example, as discussed in more detail herein, the method may comprise a step for washing the captured and infected microorganism, after adding the bacteriophage but before incubating, to remove excess parental bacteriophage and/or luciferase or other reporter protein contaminating the bacteriophage preparation.

In contrast to assays known in the art, detection of the microorganism of interest may be completed without the need for culturing the sample as a way to increase the population of the microorganisms. Thus, in certain embodiments, detection of the microorganism of interest is completed in less time than a time period required for increasing the number of microorganisms by 4-fold or 10-fold using culturing for enrichment. For example, in certain embodiments the total time required for detection is less than 6.0 hours, 5.0 hours, 4.0 hours, 3.0 hours, 2.5 hours, 2.0 hours, 1.5 hours, 1.0 hour, 45 minutes, or less than 30 minutes.

Also, in contrast to assays known in the art, the method of the invention can detect individual microorganisms. Thus, in certain embodiments, the method may detect ≤10 cells of the microorganism (i.e., 1, 2, 3, 4, 5, 6, 7, 8, 9 microorganisms) present in a sample.

Thus, aspects of the present invention provide methods for detection of microorganisms in a test sample via an indicator moiety. In some embodiments, where the microorganism of interest is a bacteria, the indicator moiety may be associated with an infectious agent such as an indicator bacteriophage. The indicator moiety may react with a substrate to emit a detectable signal or may emit an intrinsic signal (e.g., fluorescent protein). In some embodiments, the detection sensitivity can reveal the presence of as few as 50, 20, 10, 9, 8, 7, 6, 5, 4, 3, or 2 cells of the microorganism of interest in a test sample. In some embodiments, even a single cell of the microorganism of interest may yield a detectable signal.

In some embodiments, the indicator moiety associated with the infectious agent may be detectable during or after replication of the infectious agent. Many different types of detectable biomolecules suitable for use as indicator moieties are known in the art, and many are commercially available. In some embodiments the indicator phage comprises an enzyme, which serves as the indicator moiety. In some embodiments, the genome of the indicator phage is modified to encode a soluble protein. In some embodiments, the indicator phage encodes a detectable enzyme. The indicator may emit light and/or may be detectable by a color change. Various appropriate enzymes are commercially available, such as alkaline phosphatase (AP), horseradish peroxidase (HRP), or luciferase (Luc). In some embodiments, these enzymes may serve as the indicator moiety. In some embodiments, Firefly luciferase is the indicator moiety. In some embodiments, Oplophorus luciferase is the indicator moiety. In some embodiments, NANOLUC® is the indicator moiety. Other engineered luciferases or other enzymes that generate detectable signals may also be appropriate indicator moieties.

Detecting the indicator may include detecting emissions of light. In some embodiments, a luminometer may be used to detect the indicator (e.g., luciferase). However, other machines or devices may also be used. For example, a spectrophotometer, CCD camera, or CMOS camera may detect color changes and other light emissions.

In some embodiments, indicator phage is genetically engineered to contain the gene for an enzyme, such as a luciferase, which is only produced upon infection of bacteria that the phage specifically recognizes and infects. In some embodiments, the indicator moiety is expressed late in the viral life cycle. In some embodiments, as described herein, the indicator is a soluble protein (e.g., soluble luciferase) and is not fused with a phage structural protein that limits its copy number.

In various embodiments of the methods of the invention, the microorganism may be detected without any purification of the microorganisms from a sample. For example, in certain embodiments, a sample containing one or a few microorganisms of interest may be applied directly to an assay container such as a spin column, an microtiter well, or a filter and the assay is conducted in that assay container. Various embodiments of such assays are disclosed herein.

For example, aliquots of a test sample comprising bacteria may be applied to a spin column and after infection with a recombinant bacteriophage and an optional washing to remove any excess bacteriophage, the amount of soluble indicator detected will be proportional to the amount of bacteriophage that are produced by infected bacteria. Example 4 describes such an assay.

Or, aliquots of a test sample may be distributed directly into wells of a multi-well plate, indicator phage may be added, and after a period of time sufficient for infection, a lysis buffer may be added as well as a substrate for the indicator moiety (e.g., luciferase substrate for a luciferase indicator) and assayed for detection of the indicator signal. Examples 5-6 describe embodiments of the method performed on filter plates. Examples 7-9 herein describe assay variations called the “No concentration assay.”

For example, in many embodiments, multi-well plates are used to conduct the assays. The choice of plates (or any other container in which detecting may be performed) may affect the detecting step. For example, some plates may include a colored or white background, which may affect the detection of light emissions. Generally speaking, white plates have higher sensitivity but also yield a higher background signal. Other colors of plates may generate lower background signal but also have a slightly lower sensitivity. Additionally, one reason for background signal is the leakage of light from one well to another, adjacent well. There are some plates that have white wells but the rest of the plate is black. This allows for a high signal inside the well but prevents well-to-well light leakage and thus may decrease background. Thus the choice of plate or other assay vessel may influence the sensitivity and background signal for the assay.

Thus in some embodiments utilizing indicator phage, the invention comprises a method for detecting a microorganism of interest comprising the steps of capturing at least one sample microorganism; incubating the at least one microorganism with a plurality of indicator phage; allowing time for infection and replication to generate progeny phage and express soluble indicator moiety; and detecting the progeny phage, or preferably the indicator, wherein detection of the indicator demonstrates that the microorganism is present in the sample.

For example, in some embodiments the test sample microorganism may be captured by binding to the surface of a plate, or by filtering the sample through a bacteriological filter (e.g., 0.45 m pore size spin filter or plate filter). In an embodiment, the infectious agent (e.g., indicator phage) is added in a minimal volume to the captured sample directly on the filter. In an embodiment, the microorganism captured on the filter or plate surface is subsequently washed one or more times to remove excess unbound infectious agent. In an embodiment, media (e.g., Luria-Bertani also called LB broth herein) is added for further incubation time, to allow replication of phage and high-level expression of the gene encoding the indicator moiety. However, a surprising aspect of embodiments of the assays is that the incubation step only needs to be long enough for a single phage life cycle. The amplification power of using bacteriophage was previously thought to require more time, such that the phage would replicate for several cycles. A single replication of indicator phage is sufficient to facilitate sensitive and rapid detection according to some embodiments of the present invention.

Soluble indicator (e.g., luciferase) is released into the surrounding liquid upon lysis of the bacteria, which may then be measured and quantified. In an embodiment, the solution is then spun through the filter, and the filtrate collected for assay by addition of a substrate for the indicator enzyme (e.g., luciferase substrate). The filtrate may thus be removed from the capture solid support and analyzed in a new receptacle (e.g., in a luminometer), or the indicator signal may be measured directly on the filter.

In various embodiments, the purified parental indicator phage does not comprise the detectable indicator itself, because the parental phage may be purified before it is used for incubation with a test sample. Expression of late (Class III) genes occurs late in the viral life cycle. In some embodiments of the present invention, parental phage may be purified to exclude any existing indicator protein (e.g., luciferase). In some embodiments, expression of the indicator gene during progeny bacteriophage replication following infection of host bacteria results in a soluble indicator protein product. Thus, in many embodiments, it is not necessary to separate parental from progeny phage in the detecting step. In an embodiment, the microorganism is a bacterium and the indicator phage is a bacteriophage. In an embodiment, the indicator moiety is soluble luciferase, which is released upon lysis of the host microorganism.

Thus, in an alternate embodiment, the indicator substrate may be incubated with the portion of the sample that remains bound to a filter or bound to a plate surface. Accordingly, in some embodiments the solid support is a 96-well filter plate (or regular 96-well plate), and the substrate reaction may be detected by placing the plate directly in the luminometer.

For example, in an embodiment, the invention may comprise a method for detecting E. coli O157:H7 comprising the steps of: infecting cells captured on a 96-well filter plate with a plurality of parental indicator phage capable of expressing luciferase upon infection; washing excess phage away; adding LB broth and allowing time for phage to replicate and lyse the specific E. coli target (e.g., 30-90 minutes); and detecting the indicator luciferase by adding luciferase substrate and measuring luciferase activity directly in the 96-well plate, wherein detection of luciferase activity indicates that the E. coli O157:H7 is present in the sample.

In another embodiment, the invention may comprise a method for detecting E. coli O157:H7 comprising the steps of: infecting cells in liquid solution or suspension in a 96-well plate with a plurality of parental indicator phage capable of expressing luciferase upon infection; allowing time for phage to replicate and lyse the specific E. coli target (e.g., 30-90 minutes); and detecting the indicator luciferase by adding luciferase substrate and measuring luciferase activity directly in the 96-well plate, wherein detection of luciferase activity indicates that the E. coli O157:H7 is present in the sample. In such an embodiment no capturing step is necessary. In some embodiments, the liquid solution or suspension may be a consumable test sample, such as a vegetable wash. In some embodiments, the liquid solution or suspension may be vegetable wash fortified with concentrated LB broth or Nutrient Broth. In some embodiments, the liquid solution or suspension may be bacteria diluted in LB Broth.

In some embodiments, lysis of the microorganism may occur before, during, or after the detection step. Experiments suggest that infected unlysed cells may be detectable upon addition of luciferase substrate in some embodiments. Presumably, luciferase may exit cells and/or luciferase substrate may enter cells without complete cell lysis. Thus, for embodiments utilizing the spin filter system, where only luciferase released into the lysate (and not luciferase still inside intact bacteria) is analyzed in the luminometer, lysis is required for detection. However, for embodiments utilizing filter plates or 96-well plates with sample in solution or suspension, where the original plate full of intact and lysed cells is directly assayed in the luminometer, lysis is not necessary for detection.

In some embodiments, the reaction of indicator moiety (e.g., luciferase) with substrate may continue for 30 minutes or more, and detection at various time points may be desirable for optimizing sensitivity. For example, in embodiments using 96-well filter plates as the solid support and luciferase as the indicator, luminometer readings may be taken initially and at 10- or 15-minute intervals until the reaction is completed.

Surprisingly, high concentrations of phage utilized for infecting test samples (i.e., high MOI) have successfully achieved detection of very low numbers of target microorganism in a very short timeframe. The incubation of phage with a test sample in some embodiments need only be long enough for a single phage life cycle. In some embodiments, the bacteriophage concentration for this incubating step is greater than 7×10⁶, 8×10⁶, 9×10⁶, 1.0×10⁷, 1.1×10⁷, 1.2×10⁷, 1.3×10⁷, 1.4×10⁷, 1.5×10⁷, 1.6×10⁷, 1.7×10⁷, 1.8×10⁷, 1.9×10⁷, 2.0×10⁷, 3.0×10⁷, 4.0×10⁷, 5.0×10⁷, 6.0×10⁷, 7.0×10⁷, 8.0×10⁷, 9.0×10⁷, or 1.0×10⁸PFU/mL.

Success with such high concentrations of phage is surprising because the large numbers of phage were previously associated with “lysis from without,” which killed target cells and thereby prevented generation of useful signal from earlier phage assays. It is possible that the clean-up of prepared phage stock described herein helps to alleviate this problem (e.g., clean-up by cesium chloride isopycnic density gradient ultracentrifugation), because in addition to removing any contaminating luciferase associated with the phage, this clean-up may also remove ghost particles (particles that have lost DNA). The ghost particles can lyse bacterial cells via “lysis from without,” killing the cells prematurely and thereby preventing generation of indicator signal. Electron microscopy demonstrates that a crude JG04 lysate (i.e., before cesium chloride clean-up) may have greater than 50% ghosts. These ghost particles may contribute to premature death of the microorganism through the action of many phage particles puncturing the cell membrane. Thus ghost particles may have contributed to previous problems where high PFU concentrations were reported to be detrimental. Moreover, a very clean phage prep allows the assay to be performed with no wash steps, which makes the No Concentration assay possible.

Spin Column Assays

FIG. 5 shows a strategy of using indicator phage that produce soluble luciferase according to an embodiment of the invention. In this method, the phage (e.g., T7, T4, or JG04 phage) may be engineered to express a soluble luciferase during replication of the phage. Expression of luciferase is driven by a viral capsid promoter (e.g., the bacteriophage T7 or T4 late promoter), yielding high expression. Parental phage will be free of luciferase, so the luciferase detected in the assay must come from replication of progeny phage during infection of the bacterial cells. Thus, there is generally no need to separate out the parental phage from the progeny phage.

In these experiments, at least part of the sample 500 comprising the E. coli

bacteria

502 to be quantified is placed in a spin column filter and centrifuged to remove the LB broth, and an appropriate multiplicity of T7 phage 504 genetically engineered to express soluble luciferase 503 are added. The infected cells may be incubated for a time sufficient for replication of progeny phage and cell lysis to occur (e.g., 30-90 minutes at 37° C.). The parental 504 and progeny phage 516 plus free luciferase 503 in the lysate may then be collected, e.g., by centrifugation, and the level of luciferase in the filtrate quantified using a luminometer 518. Alternatively, a high through-put method may be employed where bacterial samples are applied to a 96-well filter plate, and after all manipulations listed above are performed, may be directly assayed for luciferase in the original 96-well filter plate without a final centrifugation step.

Data from example experiments of embodiments of the invention are shown in FIGS. 6-9 . The results demonstrate alternative embodiments of the invention utilizing indicator phage to assay sample bacteria via detection of soluble luciferase produced by the infection of bacteria with indicator phage. Indicator detection level calibrated as relative light units (RLU) is plotted against cell concentrations determined from the standard overnight colony forming unit (CFU) assay and expressed as “cells per assay,” thus demonstrating similar sensitivity. Increasing luciferase signal corresponds to increasing input sample cells, demonstrating a dose-dependent response.

As shown in FIG. 6 the method of the invention may demonstrate high sensitivity for detection of target bacteria using indicator phage with spin column filters. In this assay, a test sample may be collected on a spin filter by centrifugation and incubated with indicator phage comprising a gene for soluble luciferase (e.g., as shown in FIG. 1 ). Following incubation for a time sufficient for infection (e.g., 10 minutes at room temperature), the filter may be washed and spun to remove excess input phage. Media (e.g., LB broth) may be added and incubated (e.g., for 30 minutes at 37° C.) to allow replication of progeny phage and lysis of bacteria. Filters may be spun again to remove the filtrate, which may be transferred to a luminometer plate, and a luciferase assay was performed (e.g., using a Promega® luminometer with injection of Luciferase Assay Reagent, Promega, Inc.). The cell count may be corrected according to the number of colonies in the parallel CFU assay.

As shown in FIG. 6 , approximately 1,700 bacterial cells may be detected in the original sample, and further assay of serial dilutions may demonstrate detection down to an average of 1.7 cells, corresponding to actual detection of 1 or 2 cells. This shows that infection of as few as 1 to 3 E. coli cells can provide a measurable signal, via luciferase activity. This also shows statistical significance for the presence or absence of even a single cell over background (p value=0.018).

FIG. 7 demonstrates the very large detection range of the same method described for the assay of FIG. 5 using serial dilutions across a broader range of cell numbers. This shows detection may range from an average of 1.4 cells to 14 million cells.

Filter Plate Assays

As noted above, in certain embodiments, the assay may be conducted directly in the well of a microtiter assay plate. For example, FIG. 8 demonstrates the use of indicator phage with a 96-well filter plate for capture and detection. The method is the same as described above for FIG. 5 , except that the entire assay is performed in a 96-well filter plate, including the luciferase reaction. This embodiment reduces manipulations and materials compared to the spin filter method. The reduced manipulations and use of a 96-well filter plate is amenable to a high throughput assay situation, and may be adapted for use with a liquid handling robot according to embodiments of the invention. FIG. 8 shows that in this embodiment, a 96-well filter plate may be used to detect single E. coli cells (0.5 cells average assayed, confirming that about one-half of the wells received single cells), 5.4 and 54 cells.

FIG. 9 demonstrates that in certain embodiments, a very large detection range of cell concentrations may be achieved for the same assay, using the 96-well system, from less than 1 cell per assay on average (single cells) to at least 14 million cells per assay. Multiple reads at different time points after addition of the luciferase substrate may demonstrate varied sensitivity. Sensitivity for detecting <10 cells was achieved with a 15 minute read, and sensitivity down to single cell levels may be achieved at the 30 minute read. Thus time may be saved if tens of cells or less need not be detected. Note signal increases in response to increased number of input sample cells in both experiments, again demonstrating a dose-dependent response.

FIG. 10 depicts a filter plate assay for detecting bacteria of interest using a modified bacteriophage according to an embodiment of the invention. An actual experiment utilizing this assay is described in Example 6. Briefly, samples 1016 that include a bacterium of interest 1018 may be added to wells 1002 of a multi-well filter plate 1004 and spun 1006 to concentrate the samples by removal of liquid from the sample. Genetically modified phage 1020 are added to wells and incubated with additional media added for enough time sufficient for adsorption 1008 followed by infection of target bacteria and advancement of the phage life cycle 1010 (e.g., ˜45 minutes). Finally, luciferase substrate is added and reacts with any luciferase present 1024. The resulting emission is measured in a luminometer 1014 which detects luciferase activity 1026. FIG. 11 shows results from a filter plate assay as described in FIG. 10 , using JG04-NANOLUC® phage to detect E. coli O157:H7 cells in samples with known cell numbers. Student's t-Test showed a p value of 0.034 between 0 cells and 1 cell per assay, demonstrating statistical significance.

In certain embodiments, the assay may be performed without concentrating the bacterium on or near the capture surface. FIG. 12 illustrates a “No Concentration Assay” for detecting a bacterium of interest using a modified bacteriophage according to an embodiment of the invention. Aliquots of indicator phage 1214 are distributed to the individual wells 1202 of a multi-well plate 1204, and then test sample aliquots containing bacteria 1212 are added and incubated 1206 (e.g., 45 minutes at 37° C.) for a period of time sufficient for phage to replicate and generate soluble indicator 1216 (e.g., luciferase). The plate wells 1208 containing soluble indicator and phage may then be assayed 1210 to measure the indicator activity on the plate 1218 (e.g., luciferase assay). Actual experiments utilizing this method are described in Examples 7-9. In this embodiment, the test samples are not concentrated (e.g., by centrifugation) but are simply incubated directly with indicator phage for a period of time and subsequently assayed for luciferase activity.

FIG. 13 shows results from a No Concentration Assay type assay as depicted in FIG. 12 using JG04-OpLuc phage to detect E. coli O157:H7 cells in samples with known cell numbers in the low number range (i.e., very diluted cell samples). This experiment, as described in Example 7, demonstrates that statistically significant differences can be seen between the signal from 0 cells and 1 cell per assay (p value=0.0024 by ANOVA test), demonstrating the ability to detect single cells. Thus the assay is surprisingly sensitive. Samples with fewer than 1 cell per well appear to show a proportional number of wells above the background signal.

FIG. 14 shows results from a No Concentration Assay using JG04-OpLuc phage to detect E. coli O157:H7 cells in samples with known cell numbers in the very low to very high number range (i.e., samples containing less than 1 cell per assay to millions of cells). This experiment, as described in Example 8, demonstrates statistically significant differences between the signal from 0 cells and 1.1 cell per assay (p value=0.000702 by Student's t-Test), demonstrating the ability to detect single cells. More bacterial cells per assay show increasing signal in a dose dependent manner, up to at least 10⁶bacterial cells/assay, surprisingly demonstrating a very wide range of detection.

FIG. 15 shows results from a No Concentration Assay using JG04-OpLuc phage to detect E. coli O157:H7 cells in Vegetable Wash samples with known cell numbers, as described in Example 9.

To prepare the vegetable wash, vegetable leaves (e.g., spinach or lettuce) may be weighed and added to a clean plastic bag. One mL of LB (+/− 0.01-0.05% Tween®20) was added per each gram (g) of vegetable. Leaves and solution are mixed manually for a few minutes. Liquid is then extracted from the plastic bag and used as the “vegetable wash.” Using this method, ˜1 million bacteria were found to reside on a single spinach leaf (1-2 g)

The assay is quantitative in that the signal detected is proportional to the amount of the microorganism of interest in the sample. For example, in the experiment depicted in FIG. 15 , known numbers of E. coli O157:H7 cells were added to vegetable wash samples to simulate contamination of vegetables with pathogenic bacteria. The experiment using vegetable wash samples demonstrates marked differences between the signal from 0 cells and 3 cells per assay, demonstrating the ability to detect single-digit cell numbers in vegetable wash. Using more bacterial cells per assay shows increasing signal in a dose dependent manner. The vegetable wash contains about 10⁶non-target bacteria/mL, corresponding to at least 10⁵non-target bacteria per sample in this assay (including the 0 cells E. coli O157:H7 control). The ability to discern as few as 3 target bacterial cells from 10⁵non-target bacteria is surprising and again demonstrates the specificity of the assay.

Capture of the Microorganism Prior to Exposure to Infectious Agent

In some embodiments, the present invention comprises methods and systems that do not require a step for capturing microorganisms. Other embodiments allow physical isolation of bacterial cells from a sample. Methods described herein may serve as means to facilitate detection of low levels of a microorganism (e.g., a single microorganism) present in a sample. A capturing step may be based on a specific binding agent, such as an antibody that recognizes the microorganism of interest, or it may be based on selection for other features of the microorganism, such as size fractionation.

In some embodiments, a microorganism is captured based on physical features other than molecular specificity (e.g., size). In some embodiments, the present invention utilizes the physical size of the microorganism to capture it on a solid support. In some embodiments, the solid support is a filter. For example, filtering a sample through a bacteriological filter (e.g., 0.45 μm pore size spin filter) allows smaller substances to pass through while retaining intact bacteria. Alternatively, a plate filter may be used to capture a microorganism, or a variety of other filter devices may be used (e.g., 96-well filter plate).

For example, the method may include the step of collecting the microorganism on a solid support, such as for example by filtering a sample through a bacteriological filter. After size-based capture, any binding agent that specifically targets the microorganism of interest may be employed. For example, an infectious agent may be incubated with the captured microorganism, in order to specifically target and identify the microorganism of interest. Other methods of isolating the microorganisms in the sample may be used. In some embodiments, detection steps may be performed before, simultaneously with, or after such capture steps.

In some embodiments, binding agents with high specificity for a microorganism of interest may be employed as a means to facilitate specific capture of low levels of a microorganism (e.g., a single microorganism) present in a sample. In some embodiments, a large volume of liquid sample to be tested may need to be effectively concentrated before further testing.

For example, a single bacterium, which may have a volume of about one cubic micrometer, can be isolated from a one-milliliter sample having a volume of 10¹²cubic micrometers. In such embodiments the capturing step may comprise contacting the sample with a plurality (an excess) of affinity-purified capture antibodies or antibody fragments.

Some embodiments utilize affinity-purified and/or reverse-purified surface-specific antibodies or antibody fragments generated against antigenic molecules found on the surface of a specific microorganism of interest. Such antibodies or antibody fragments can specifically identify a microorganism for capture or detection purposes or both. Antibodies demonstrating specific recognition of surface antigens on a wide variety of bacteria or other microorganisms are available commercially from a number of sources, such as Kirkegaard & Perry Laboratories, Inc. (KPL) or Abcam.

In some embodiments of the invention, affinity-purified and/or reverse-purified surface-specific antibodies that recognize the microbial surface antigens of a particular microorganism (e.g., E. coli O157:H7) do not recognize other similar microorganisms (e.g., E. coli B). In some embodiments, antibodies specific to, e.g., E. coli B or E. coli O157:H7 do not recognize cells of Salmonella typhimurium or Staphylococcus epidermidis. This represents another surprising discovery, as many bacteria have, e.g., surface lipopolysaccharide (Gram-negative bacteria) or lipoteichoic acid (Gram-positive bacteria) molecules that were previously believed to be highly similar, especially between closely related species.

Methods for antibody-based capture disclosed herein may be adapted to any bacterium or other microorganism of interest (e.g. pathogenic microorganisms) for which surface-specific antibodies are available which do not cross-react with other microorganisms.

For example, in some embodiments, a capturing step of the invention may use capture antibodies or antibody fragments that are specific for the microorganism to facilitate capture of the microorganism. In some embodiments, capture antibodies may be conjugated to a chemical moiety that binds with another binding agent attached to a solid support (e.g. beads or a plate surface). For example, in some embodiments, the capture antibody may be biotinylated to facilitate binding to streptavidin bound to a solid support. In some embodiments, the solid support comprises magnetic beads. In other embodiments, a solid support comprises a plate surface or the surfaces of a multi-well plate (e.g., an ELISA plate). For example, an ELISA plate may be coated with an antibody that specifically recognizes the microorganism of interest.

In certain embodiments, the microorganism may be isolated from other components of the sample through binding of the microorganism to a free capture antibody or antibody fragment that subsequently binds to a solid support. In some embodiments, the capture antibody or antibody fragment comprises a binding agent (e.g., biotin) that binds to a second agent (e.g., streptavidin) bound to a solid support.

In some embodiments, e.g., if the capture antibody is labeled with biotin, the method may further comprise contacting the sample with a plurality of magnetic streptavidin-coated beads to bind the bacterium-antibody complex, and sequestering the bead-antibody-bacterium complex with a magnet to isolate the bacteria. Or, other methods of purifying the biotin-antibody: bacterium complex may be used. With such embodiments, a bacterium in a one-milliliter sample can be concentrated to about one microliter (˜1000-fold), facilitating further detection and/or quantification by methods described herein.

Thus, in some embodiments, the invention comprises a method for detecting a microorganism of interest wherein the capture step comprises specifically isolating the microorganism from other components in the sample.

Alternatively, in some embodiments the capturing step may be based on other features of the microorganism of interest, such as size. In embodiments utilizing size-based capture, the solid support may be a spin column filter. In some embodiments, the solid support comprises a 96-well filter plate. Or, the solid support for capture may be a location on an array, or a mobile support, such as a bead.

Thus, in some embodiments, a target microorganism may be captured and isolated from a large volume before detection using the methods described above. For example, the microorganism may be specifically isolated using attributes of a capture antibody or antibody fragment. In some embodiments, the capture antibody is biotinylated such that it facilitates subsequent binding of cell-antibody complexes to magnetic streptavidin beads. The biotin on the antibody can bind tightly to the streptavidin on the magnetic bead. Or the capture antibody may be conjugated to another protein or other molecule, which facilitates capture on beads or another solid support. Such embodiments may provide increased sensitivity, particularly where the initial sample volume is large. Thus, the method may comprise the steps of attaching a plurality of binding agents that can specifically bind to a surface antigen on the microorganism of interest, which thereby facilitates binding to a capture solid support.

Alternatively, another chemical moiety that binds the anti-bacterium antibody may be used to coat magnetic beads. For example, a bead coated with a secondary antibody that recognizes or binds the anti-bacterium antibody may be used. The bacteria bound to the beads may then be isolated. In an embodiment, the efficiency of capture may be quantified by plating the bacteria bound to the beads and the unbound supernatant fraction and counting the resultant colonies (CFU). In other embodiments, the signal generated by reaction with substrate (i.e., substrate reagent for the indicator moiety) is measured for detection.

In some embodiments, the specificity of antibodies is demonstrated using specific capture on a solid support. A method of the invention may comprise the step of retrieving and concentrating a microorganism (e.g., a bacterium) from a sample by the use of a substrate with a binding agent specific for the microorganism. In an embodiment, the binding agent is immobilized on a solid support (e.g. magnetic beads) or is free and subsequently immobilized on a solid support. The immobilized microorganism may then be removed from the sample (e.g., by aspiration, decanting, magnetic force, or other appropriate isolation techniques) and detected by a variety of techniques.

FIG. 16 depicts an example embodiment of specific capture of E. coli O157:H7 but not E. coli B or S. typhimurium from samples by the use of antibodies produced against intact E. coli O157:H7. Thus, in certain embodiments magnetic beads coated with streptavidin may be used to isolate E. coli O157:H7 preincubated with free biotinylated polyclonal antibodies (KPL), affinity-purified and reverse-purified to minimize cross-reactivity with other microbial species. In certain embodiments, the E. coli O157:H7 will only be present in the captured fraction (i.e., bead fraction) when specific E. coli O157:H7 antibodies were used, and no bacteria will be recovered in the supernatant (unbound) fraction. In certain embodiments, E. coli B and S. typhimurium cells are found only in the supernatant fraction when E. coli O157:H7-specific antibodies are used, illustrating the remarkable specificity of these antibodies. In the absence of antibody, all three types of bacteria were found in the supernatant fraction.

Hybrid Immuno-Phage (HIP) Assay

In certain embodiments, the methods of the present invention combine the use of a binding agent (e.g., antibody) to purify and/or concentrate a microorganism of interest from the sample in addition to detection with an infectious agent. For example, in certain embodiments, the present invention comprises a method for detecting a microorganism of interest in a sample comprising the steps of: capturing the microorganism from the sample on a prior support using a capture antibody specific to the microorganism of interest; incubating the sample with a recombinant bacteriophage that infects the microorganism of interest, wherein the recombinant bacteriophage comprises an indicator gene inserted into a late gene region of the bacteriophage such that expression of the indicator gene during bacteriophage replication following infection of host bacteria results in a soluble indicator protein product; and detecting the indicator protein product, wherein positive detection of the indicator protein product indicates that the microorganism of interest is present in the sample.

For example, FIG. 17 depicts a Hybrid Immuno-Phage (HIP) Assay for detecting a bacterium of interest using a modified bacteriophage according to an embodiment of the invention. The sample is first applied to the microtiter plate well coated with bacterium-specific antibodies 1702. The plate is then centrifuged to facilitate binding of the bacterium to the capture antibodies 1704. Following sufficient time to allow for complete bacteria capture, a solution containing bacterium-specific NANOLUC®-phage is added to each sample 1706. Incubation with the phage results in the binding and attachment of a single or multiple phages to the captured bacterium 1708. Finally, the sample is incubated to facilitate phage replication and luciferase expression, which leads to cell lysis and release of soluble luciferase 1710.

FIG. 18 shows results from a HIP assay using JG04-NANOLUC® phage to detect E. coli O157:H7 cells in samples with known cell numbers, as described in Example 11, on a log scale. The HIP assay was able to detect 100 and 1,000 E. coli O157:H7 cells in LB media with approximately 2×10⁶PFU JG04-NANOLUC® phage. The average signal over a no-cell sample ranged from approximately 50-fold for the 100 cell sample to over 1,000-fold for the 1,000 cell sample.

In some embodiments, the incubating step of the methods described herein comprises a final bacteriophage concentration of greater than 7×10⁶, 8×10⁶, 9×10⁶, 1.0×10⁷, 1.1×10⁷, 1.2×10⁷, 1.3×10⁷, 1.4×10⁷, 1.5×10⁷, 1.6×10⁷, 1.7×10⁷, 1.8×10⁷, 1.9×10⁷, 2.0×10⁷, 3.0×10⁷, 4.0×10⁷, 5.0×10⁷, 6.0×10⁷, 7.0×10⁷, 8.0×10⁷, 9.0×10⁷, or 1.0×10⁸PFU/mL. This high phage concentration was previously purported to be detrimental to such an assay, and thus yields surprising results. In some embodiments, the methods of the invention require less than 3 hours, less than 2.5 hours, less than 2 hours, less than 1.5 hours, or less than 1 hour for detection of a microorganism of interest. In some embodiments, the methods can detect as few as 100, 50, 20, 10, 9, 8, 7, 6, 5, 4, 3, or 2 cells of the microorganism of interest. These are shorter timeframes than were previously thought possible. In some embodiments, even a single cell of the microorganism is detectable. In additional embodiments, the invention comprises systems (e.g., computer systems, automated systems or kits) comprising components for performing the methods disclosed herein, and/or using the modified infectious agents described herein.

Systems and Kits of the Invention

In some embodiments, the invention comprises systems (e.g., automated systems or kits) comprising components for performing the methods disclosed herein. Some embodiments described herein are particularly suitable for automation or kits, given the minimal amount of reagents and materials required to perform the methods. In certain embodiments, each of the components of the a kit may comprise a self-contained unit that is deliverable from a first site to a second site.

In some embodiments, the invention comprises a systems or kits for rapid detection of a microorganism of interest in a sample. The systems or kits may in certain embodiments comprise a component for incubating the sample with an infectious agent specific for the microorganism of interest, wherein the infectious agent comprises an indicator moiety and a component for detecting the indicator moiety. In some embodiments of both the systems and the kits of the invention, the infectious agent is a recombinant bacteriophage that infects the microorganism of interest, and the recombinant bacteriophage comprises an indicator gene inserted into a late gene region of the bacteriophage as the indicator moiety such that expression of the indicator gene during bacteriophage replication following infection of host bacteria results in a soluble indicator protein product. Some systems further comprise a component for capturing the microorganism of interest on a solid support.

In certain embodiments, the systems and/or kits may further comprise a component for washing the captured microorganism sample. Additionally or alternatively, the systems and/or kits may further comprise a component for determining amount of the indicator moiety, wherein the amount of indicator moiety detected corresponds to the amount of microorganism in the sample. For example, in certain embodiments, the system or kit may comprise a luminometer or other device for measuring a luciferase enzyme activity.

In some systems and/or kits, the same component may be used for multiple steps. In some systems and/or kits, the steps are automated or controlled by the user via computer input and/or wherein a liquid-handling robot performs at least one step.

Thus in certain embodiments, the invention may comprise a system for rapid detection of a microorganism of interest in a sample, the system comprising: a component for incubating the sample with an infectious agent specific for the microorganism of interest, wherein the infectious agent comprises an indicator moiety; a component for capturing the microorganism from the sample on a solid support; a component for washing the captured microorganism sample to remove unbound infectious agent; and a component for detecting the indicator moiety. In some embodiments, the same component may be used for steps of capturing and/or incubating and/or washing. Some embodiments additionally comprise a component for determining amount of the microorganism of interest in the sample, wherein the amount of indicator moiety detected corresponds to the amount of microorganism in the sample. Such systems can include various embodiments and subembodiments analogous to those described above for methods of rapid detection of microorganisms. In an embodiment, the microorganism is a bacterium and the infectious agent is a bacteriophage. In a computerized system, the system may be fully automated, semi-automated, or directed by the user through a computer (or some combination thereof).

In some embodiments, the system may comprise a component for isloated the microorganism of interest from the other components in the sample.

In an embodiment, the invention comprises a system comprising components for detecting a microorganism of interest comprising: a component for isolating at least one microorganism from other components in the sample; a component for infecting the at least one microorganism with a plurality of a parental infectious agent; a component for lysing the at least one infected microorganism to release progeny infectious agents present in the microorganism; and a component for detecting the progeny infectious agents, or a constituent of the progeny infectious agents, wherein detection of the infectious agent or a constituent of the infectious agent, indicates that the microorganism is present in the sample.

The systems may comprise a variety of components for detection of progeny infectious agents. For example, in an embodiment, the progeny infectious agent (e.g., bacteriophage) may comprise an indicator moiety. In an embodiment, the indicator moiety in the progeny infectious agent (e.g., bacteriophage) may be a detectable moiety that is expressed during replication, such as a soluble luciferase protein.

In other embodiments, the invention may comprise a kit for rapid detection of a microorganism of interest in a sample, the system comprising: a component for incubating the sample with an infectious agent specific for the microorganism of interest, wherein the infectious agent comprises an indicator moiety; a component for capturing the microorganism from the sample on a solid support; a component for washing the captured microorganism sample to remove unbound infectious agent; and a component for detecting the indicator moiety. In some embodiments, the same component may be used for steps of capturing and/or incubating and/or washing. Some embodiments additionally comprise a component for determining amount of the microorganism of interest in the sample, wherein the amount of indicator moiety detected corresponds to the amount of microorganism in the sample. Such kits can include various embodiments and subembodiments analogous to those described above for methods of rapid detection of microorganisms. In an embodiment, the microorganism is a bacterium and the infectious agent is a bacteriophage.

In some embodiments, the kit may comprise a component for isolated the microorganism of interest from the other components in the sample.

In an embodiment, the invention comprises a kit comprising components for detecting a microorganism of interest comprising: a component for isolating at least one microorganism from other components in the sample; a component for infecting the at least one microorganism with a plurality of a parental infectious agent; a component for lysing the at least one infected microorganism to release progeny infectious agents present in the microorganism; and a component for detecting the progeny infectious agents, or a constituent of the progeny infectious agents, wherein detection of the infectious agent or a constituent of the infectious agent, indicates that the microorganism is present in the sample.

The kits may comprise a variety of components for detection of progeny infectious agents. For example, in an embodiment, the progeny infectious agent (e.g., bacteriophage) may comprise an indicator moiety. In an embodiment, the indicator moiety in the progeny infectious agent (e.g., bacteriophage) may be a detectable moiety that is expressed during replication, such as a soluble luciferase protein.

These systems and kits of the invention include various components. As used herein, the term “component” is broadly defined and includes any suitable apparatus or collections of apparatuses suitable for carrying out the recited method. The components need not be integrally connected or situated with respect to each other in any particular way. The invention includes any suitable arrangements of the components with respect to each other. For example, the components need not be in the same room. But in some embodiments, the components are connected to each other in an integral unit. In some embodiments, the same components may perform multiple functions.

Computer Systems and Computer Readable Media

The system, as described in the present technique or any of its components, may be embodied in the form of a computer system. Typical examples of a computer system include a general-purpose computer, a programmed microprocessor, a microcontroller, a peripheral integrated circuit element, and other devices or arrangements of devices that are capable of implementing the steps that constitute the method of the present technique.

A computer system may comprise a computer, an input device, a display unit, and/or the Internet. The computer may further comprise a microprocessor. The microprocessor may be connected to a communication bus. The computer may also include a memory. The memory may include random access memory (RAM) and read only memory (ROM). The computer system may further comprise a storage device. The storage device can be a hard disk drive or a removable storage drive such as a floppy disk drive, optical disk drive, etc. The storage device can also be other similar means for loading computer programs or other instructions into the computer system. The computer system may also include a communication unit. The communication unit allows the computer to connect to other databases and the Internet through an I/O interface. The communication unit allows the transfer to, as well as reception of data from, other databases. The communication unit may include a modem, an Ethernet card, or any similar device which enables the computer system to connect to databases and networks such as LAN, MAN, WAN and the Internet. The computer system thus may facilitate inputs from a user through input device, accessible to the system through I/O interface.

A computing device typically will include an operating system that provides executable program instructions for the general administration and operation of that computing device, and typically will include a computer-readable storage medium (e.g., a hard disk, random access memory, read only memory, etc.) storing instructions that, when executed by a processor of the server, allow the computing device to perform its intended functions. Suitable implementations for the operating system and general functionality of the computing device are known or commercially available, and are readily implemented by persons having ordinary skill in the art, particularly in light of the disclosure herein.

The computer system executes a set of instructions that are stored in one or more storage elements, in order to process input data. The storage elements may also hold data or other information as desired. The storage element may be in the form of an information source or a physical memory element present in the processing machine.

The environment can include a variety of data stores and other memory and storage media as discussed above. These can reside in a variety of locations, such as on a storage medium local to (and/or resident in) one or more of the computers or remote from any or all of the computers across the network. In a particular set of embodiments, the information may reside in a storage-area network (“SAN”) familiar to those skilled in the art. Similarly, any necessary files for performing the functions attributed to the computers, servers, or other network devices may be stored locally and/or remotely, as appropriate. Where a system includes computing devices, each such device can include hardware elements that may be electrically coupled via a bus, the elements including, for example, at least one central processing unit (CPU), at least one input device (e.g., a mouse, keyboard, controller, touch screen, or keypad), and at least one output device (e.g., a display device, printer, or speaker). Such a system may also include one or more storage devices, such as disk drives, optical storage devices, and solid-state storage devices such as random access memory (“RAM”) or read-only memory (“ROM”), as well as removable media devices, memory cards, flash cards, etc.

Such devices also can include a computer-readable storage media reader, a communications device (e.g., a modem, a network card (wireless or wired), an infrared communication device, etc.), and working memory as described above. The computer-readable storage media reader can be connected with, or configured to receive, a computer-readable storage medium, representing remote, local, fixed, and/or removable storage devices as well as storage media for temporarily and/or more permanently containing, storing, transmitting, and retrieving computer-readable information. The system and various devices also typically will include a number of software applications, modules, services, or other elements located within at least one working memory device, including an operating system and application programs, such as a client application or Web browser. It should be appreciated that alternate embodiments may have numerous variations from that described above. For example, customized hardware might also be used and/or particular elements might be implemented in hardware, software (including portable software, such as applets), or both. Further, connection to other computing devices such as network input/output devices may be employed.

Non-transient storage media and computer readable media for containing code, or portions of code, can include any appropriate media known or used in the art, including storage media and communication media, such as but not limited to volatile and non-volatile, removable and non-removable media implemented in any method or technology for storage and/or transmission of information such as computer readable instructions, data structures, program modules, or other data, including RAM, ROM, EEPROM, flash memory or other memory technology, CD-ROM, digital versatile disk (DVD) or other optical storage, magnetic cassettes, magnetic tape, magnetic disk storage or other magnetic storage devices, or any other medium which can be used to store the desired information and which can be accessed by the a system device. Based on the disclosure and teachings provided herein, a person of ordinary skill in the art will appreciate other ways and/or methods to implement the various embodiments.

A computer-readable medium may comprise, but is not limited to, an electronic, optical, magnetic, or other storage device capable of providing a processor with computer-readable instructions. Other examples include, but are not limited to, a floppy disk, CD-ROM, DVD, magnetic disk, memory chip, ROM, RAM, SRAM, DRAM, content-addressable memory (“CAM”), DDR, flash memory such as NAND flash or NOR flash, an ASIC, a configured processor, optical storage, magnetic tape or other magnetic storage, or any other medium from which a computer processor can read instructions. In one embodiment, the computing device may comprise a single type of computer-readable medium such as random access memory (RAM). In other embodiments, the computing device may comprise two or more types of computer-readable medium such as random access memory (RAM), a disk drive, and cache. The computing device may be in communication with one or more external computer-readable mediums such as an external hard disk drive or an external DVD drive.

As discussed above, the embodiment comprises a processor which is configured to execute computer-executable program instructions and/or to access information stored in memory. The instructions may comprise processor-specific instructions generated by a compiler and/or an interpreter from code written in any suitable computer-programming language including, for example, C, C++, C #, Visual Basic, Java, Python, Perl, JavaScript, and ActionScript (Adobe Systems, Mountain View, Calif.). In an embodiment, the computing device comprises a single processor. In other embodiments, the device comprises two or more processors. Such processors may comprise a microprocessor, a digital signal processor (DSP), an application-specific integrated circuit (ASIC), field programmable gate arrays (FPGAs), and state machines. Such processors may further comprise programmable electronic devices such as PLCs, programmable interrupt controllers (PICs), programmable logic devices (PLDs), programmable read-only memories (PROMs), electronically programmable read-only memories (EPROMs or EEPROMs), or other similar devices.

The computing device comprises a network interface. In some embodiments, the network interface is configured for communicating via wired or wireless communication links. For example, the network interface may allow for communication over networks via Ethernet, IEEE 802.11 (Wi-Fi), 802.16 (Wi-Max), Bluetooth, infrared, etc. As another example, network interface may allow for communication over networks such as CDMA, GSM, UMTS, or other cellular communication networks. In some embodiments, the network interface may allow for point-to-point connections with another device, such as via the Universal Serial Bus (USB), 1394 FireWire, serial or parallel connections, or similar interfaces. Some embodiments of suitable computing devices may comprise two or more network interfaces for communication over one or more networks. In some embodiments, the computing device may include a data store in addition to or in place of a network interface.

Some embodiments of suitable computing devices may comprise or be in communication with a number of external or internal devices such as a mouse, a CD-ROM, DVD, a keyboard, a display, audio speakers, one or more microphones, or any other input or output devices. For example, the computing device may be in communication with various user interface devices and a display. The display may use any suitable technology including, but not limited to, LCD, LED, CRT, and the like.

The set of instructions for execution by the computer system may include various commands that instruct the processing machine to perform specific tasks such as the steps that constitute the method of the present technique. The set of instructions may be in the form of a software program. Further, the software may be in the form of a collection of separate programs, a program module with a larger program or a portion of a program module, as in the present technique. The software may also include modular programming in the form of object-oriented programming. The processing of input data by the processing machine may be in response to user commands, results of previous processing, or a request made by another processing machine.

While the present invention has been disclosed with references to certain embodiments, numerous modifications, alterations and changes to the described embodiments are possible without departing from the scope and spirit of the present invention, as defined in the appended claims. Accordingly, it is intended that the present invention not be limited to the described embodiments, but that it have the full scope defined by the language of the following claims, and equivalents thereof.

Some of the embodiments of the technology described herein can be defined according to any of the following numbered paragraphs:

(1) A recombinant bacteriophage comprising an indicator gene inserted into a late gene region of the bacteriophage, and optionally wherein the late gene region is a class III gene region, and optionally wherein transcription of the indicator gene is controlled by a bacteriophage class III or “late” promoter.

(2) The recombinant bacteriophage of paragraph 1, wherein the bacteriophage is derived from T7, T4, T4-like, JG04, or another natural bacteriophage having a genome with at least 90% homology to T7, JG04, T4, or other T4-like phage; and/or wherein the amount of indicator moiety detected corresponds to the amount of the microorganism of interest present in the sample.

(3) The bacteriophage of any of paragraphs 1-2, wherein the indicator gene does not encode a fusion protein and/or wherein the indicator gene is adjacent to a major capsid gene, and optionally wherein expression of the indicator gene during bacteriophage replication following infection of a host bacterium results in a soluble indicator protein product.

(4) The bacteriophage of any of paragraphs 1-3, wherein the indicator gene encodes a luciferase enzyme, and optionally wherein the luciferase is one of Oplophorus luciferase, Firefly luciferase, or an engineered luciferase.

(5) A method for detecting a microorganism of interest in a sample comprising the steps of: incubating the sample with a recombinant bacteriophage that infects the microorganism of interest, wherein the recombinant bacteriophage comprises an indicator gene inserted into a late gene region of the bacteriophage such that expression of the indicator gene during bacteriophage replication following infection of host bacteria results in a soluble indicator protein product; and detecting the indicator protein product, wherein positive detection of the indicator protein product indicates that the microorganism of interest is present in the sample.

(6) The method of paragraph 5, wherein the late gene region is a class III gene region, and optionally wherein transcription of the indicator gene is controlled by a bacteriophage class III promoter.

(7) The method of

paragraph

5 or 6, wherein the bacteriophage is derived from T7, T4, T4-like, JG04, or another natural bacteriophage having a genome with at least 90% homology to T7, T4 or other T4-like phage, and/or wherein the amount of indicator moiety detected corresponds to the amount of the microorganism of interest present in the sample.

(8) The method of any of paragraphs 5-7, wherein the indicator gene does not encode a fusion protein and/or wherein the indicator gene is adjacent to a major capsid gene, and optionally wherein expression of the indicator gene during bacteriophage replication following infection of a host bacterium results in a soluble indicator protein product.

(9) The method of any of paragraphs 5-8, wherein the indicator gene encodes a luciferase enzyme, and optionally wherein the luciferase is one of Oplophorus luciferase, Firefly luciferase, or an engineered luciferase.

(10) The method of any of paragraphs 5-9, wherein the bacteriophage concentration for the incubating step is greater than 1×10⁷PFU/mL, and optionally wherein the recombinant bacteriophage is purified using cesium chloride isopycnic density gradient centrifugation prior to incubation with the sample.

(11) The method of any of paragraphs 5-10, further comprising a step for capturing the microorganism from the sample on a solid support before the incubating step; and optionally wherein the solid support comprises a multi-well plate or a filter; and optionally wherein the capturing step further comprises binding microorganism with a capture antibody; and optionally wherein the capture antibody facilitates binding of the microorganism to the solid support; and optionally wherein the method further comprises a step for washing the captured and infected microorganism, after adding the bacteriophage but before incubating, to remove excess bacteriophage and/or contaminating reporter protein, such as luciferase.

(12) The method of any of paragraphs 5-11, wherein detection of the microorganism of interest is completed in less time than a time period required for increasing the number of microorganisms by 4-fold or 10-fold using culturing for enrichment; and optionally wherein the method can detect ≤10 cells of the microorganism in the sample; and optionally wherein the total time required for detection is less than 2 hours.

(13) A system for rapid detection of a microorganism of interest in a sample, comprising: a component for incubating the sample with an infectious agent specific for the microorganism of interest, wherein the infectious agent comprises an indicator moiety; and a component for detecting the indicator moiety; and optionally further comprising a component for determining amount of the microorganism of interest in the sample, wherein the amount of indicator moiety detected corresponds to the amount of microorganism in the sample; and optionally further comprising a component for capturing the microorganism of interest on a solid support, and/or further comprising a component for washing the captured microorganism sample, and optionally wherein the same component may be used for multiple steps.

(14) The system of paragraph 13, wherein the infectious agent is a recombinant bacteriophage that infects the microorganism of interest, wherein the recombinant bacteriophage comprises an indicator gene inserted into a late gene region of the bacteriophage as the indicator moiety such that expression of the indicator gene during bacteriophage replication following infection of host bacteria results in a soluble indicator protein product; and optionally wherein the steps are automated or controlled by the user via computer input and/or wherein a liquid-handling robot performs at least one step; or wherein the system comprises a kit.

(15) Non-transient computer readable media for use with the method of any of paragraphs 5-12 and/or the system of any of paragraphs 13-14.

EXAMPLES

Results depicted in the following examples, except for example 11, were obtained without culturing for enrichment or without incubation of the sample to achieve replication of sample cells. Further, in the “no concentration assay,” indicator phage added directly to a sample, without concentrating the cells, could infect and detect a low number of cells, even a single bacterium.

Example 1. Creation of Indicator Phage

Indicator Phage were created using the T7SELECT®415-1 phage display system from Millipore, Inc. Briefly, purified T7SELECT® DNA was purchased and digested with DNA restriction enzymes EcoRI and HindIII (New England Biolabs®), and the cut DNA was subsequently purified. The gene for wild-type Firefly luciferase (from the common Eastern firefly, Photinus pyralis) was synthesized with a bacteriophage T7 upstream region including the late T7 promoter, to ensure high levels of expression of the luciferase gene.

The synthesized luciferase gene is designated SEQ ID NO. 1. This gene was amplified by PCR to include compatible restriction enzyme recognition sites for EcoRI and HindIII to ensure the new gene could be inserted into the T7SELECT®415-1 genome, using the following primers:

TATCTGAATTCTAAGTAACTGATAATACGACTCACTATAGGGAGACCACAA

C, designated SEQ ID NO. 2, and

AATGA

TTACAATTTGGACTTTCCGCCCTTCTTGG,

designated SEQ ID NO. 3.

Additionally, stop codons in all 3 reading frames were added upstream of the luciferase start site, to terminate production of the bacteriophage major capsid protein, the gene 10B product. The T7SELECT®415-1 phage display system is designed to create a fusion product of the gene 10B major capsid protein and any small protein inserted downstream of it. The addition of the stop codons ensures no fusion product is made, and allows the relatively large luciferase gene to be expressed in soluble form. The PCR product was digested with EcoR1 and HindIII, purified, and ligated into the T7SELECT®415-1. The ligation product was inserted into MegaX DH10B electrocompetent cells (Invitrogen®) using a Bio-Rad MicroPulser™ electroporation system, and the culture plated on E. coli for plaques. Plaques were picked, and phage were grown in E. coli DH10B and purified via sucrose density gradient centrifugation for use as Indicator Phage, T7SELECT®415-Luc.

FIG. 1 depicts the genomic structure of an example Indicator Phage, T7SELECT®415-Luc. The detectable indicator moiety is encoded by the Firefly luciferase gene inserted within the Class III gene region, expressed late in the viral life cycle and at higher levels than other phage genes. The construct contains stop codons to ensure the luciferase is not incorporated into a native gene product, such as the capsid protein gene 10B, and is thus also not a fusion protein. Thus this construct allows progeny phage to express soluble Firefly luciferase as the indicator to be detected.

Example 2. Isolation and Purification of E. coli O157:H7 Specific Bacteriophage from the Environment

Samples from the Hyperion Sewage Treatment Plant were obtained along with water samples from the neighboring Ballona wetlands. The samples were mixed with powdered Nutrient Broth (Gibco, Inc.) to 1× and inoculated with E. coli O157:H7 (ATCC 43888) from 3 mL of turbid culture. The sample was incubated for 3 hours @ 37° C. with shaking to enrich for phage that infect E. coli O157:H7, lysed with 120 μL chloroform, vortexed for 15 seconds, and a 1 mL sample was centrifuged for 2 minutes at 6800 g. The supernatants were filtered (0.45 μm filter) and plated for plaques on E. coli O157:H7. This sample was plated out in plaque assays in various dilutions to obtain well isolated plaques. Individual plaques were stabbed with disposable pipette tips and resuspended in 100 μL TMS buffer (50 mM Tris-HCl, pH 7.4, 10 mM MgCl₂, and 100 mM NaCl).

Aliquots of 5 μL of resuspended plaques were spot-tested in overlay agar on E. coli strains O157:H7, B, and DH10B, and on a strain of Salmonella. Phage that only cleared O157:H7 were amplified in E. coli O157:H7, the lysates clarified by centrifugation, and the particles put into TMS buffer using ZEBA® Buffer Exchange columns.

Eight closely related phage isolates were grown on E. coli O157:H7, purified, and the genomes isolated and sequenced. Three genomic types all showed 98% homology to the T4-like phage RB69. The late genes were mapped based on this homology, and phage JG04 was selected for further study. FIG. 2 shows JG04, and the genome of JG04 is designated SEQ ID NO. 4.

Example 3. Creation and Purification of Recombinant Indicator Phage

Based on sequence analysis and location of the late gene region, homologous recombination sequences were synthesized with inserts for various reporter genes, consisting of different luciferase proteins, as shown in FIG. 3 . Specifically, three constructs were used: Firefly luciferase homologous recombination plasmid, pUC57.HR.Fluc, corresponding to SEQ ID NO. 5; NANOLUC® Homologous Recombination Plasmid, pUC57.HR.NANOLUC® corresponding to SEQ ID NO. 6; and Oplophorus Luciferase Homologous Recombination Plasmid, pUC19.HR.OpLuc.KanR, corresponding to SEQ ID NO. 7.

Luciferase genes were inserted with an upstream T4 late gene promoter, to ensure expression during the viral late stage. In some cases, a kanamycin resistance marker was also inserted to allow for selection of infected cells under the kanamycin antibiotic. These regions were flanked with up to 500 bp of sequence matching the capsid proteins, gp23 and gp24. These synthesized sequences were carried by the Ampicillin resistant pUC57 or pUC19 plasmid.

Plasmids containing the synthesized sequences were transformed into electroporation competent E. coli O157:H7 using a BIORAD® Gene Pulser® II electroporator, conferring resistance to Ampicillin. Colonies were screened for positive transformation by assaying with the appropriate luciferase substrate (D-luciferin for Firefly luciferase, coelenterazine for Oplophorus luciferase, and either coelenterazine or NANOGLO® for NANOLUC®). E. coli O157:H7 harboring a plasmid with iuc flanked by sequences homologous with phage JG04 were grown in Ampicillin-containing LB broth bacterial cultures were grown in Ampicillin containing LB broth to approximately 10⁷cells/mL. Cultures were then infected with phage JG04 at an MOI of 1 and incubated for 45 minutes at 37° C. with shaking to lyse cells. Lysates contained a mixture of mostly wild-type phage with a minority of recombinant phage created by homologous recombination of the wild-type phage genome with the homologous recombination plasmid.

In order to determine the ratio of recombinant to wild-type phage, limiting dilution assays based on the TCID50 (tissue culture infectious dose 50%) were used to both determine the concentration of infectious units (IU/mL), akin to number of virus particles or plaque forming units, and to determine the number of luciferase transducing units (TU/mL). In these assays, the sample was serially diluted, with each dilution aliquoted into replicates wells with E. coli O157:H7 bacteria. Any wells that show luciferase activity must have been infected with at least one recombinant phage. Any wells that showed cell lysis had been infected by at least one phage. Based on the highest dilution where each of these cases occurred, the original concentrations were back-calculated. These initial phage mixtures from transformed cells typically yielded a ratio of 20,000 wild-type IU for each recombinant phage TU. Steps were then taken to isolate and amplify the recombinant phage.

As illustrated in FIG. 4 , recombinant phage were isolated from a mixture comprising 0.005% of total phage. The phage mixtures were diluted into 96 well plates to give an average of 3 recombinant TU per plate, which breaks down to about 625 IU of mostly wild-type phage per well. Each well contained 50 μL of turbid E. coli O157:H7. After 2 hours of incubation at 37° C., wells were sampled and screened for the presence of luciferase. Any positive wells would likely have been inoculated with a single recombinant phage, and ˜600 wild-type phage, which is an enrichment over the original 20,000:1 ratio. Progeny from this enriched culture was subjected to another limiting dilution assay to verify the ratio and determine the actual concentration of recombinant phage transducing units.

Again, 3 recombinant TU per 96-well plate were aliquoted from this stock, leading to an approximate inoculation of ˜20 mostly wild-type phage per well. Any positive luciferase wells were likely to have been inoculated with a single recombinant along with ˜20 wild-type phage. These wells were analyzed for luciferase activity, and any positive wells were subjected to the limiting dilution assay to determine the ratio of TU to IU, then to plaque assay to obtain well-isolated plaques.

At this point, the expected ratio of wild-type to recombinants was about 20:1.48 plaques were individually picked and screened for luciferase transducing ability, insuring about 3 recombinants were in the mix of plaques being screened. Each plaque was suspended in 100 μL TMS, and 5 μL was added to a well containing a turbid E. coli O157:H7 culture, and wells were assayed after incubation for 45 minutes to 1 hour at 37° C.

Positive wells were expected to contain a pure culture of recombinant phage, but an additional round of plaque purification was standard procedure. Large scale production was performed to obtain high titer stocks appropriate for use in the E. coli O157:H7 detection assay. Cesium chloride isopycnic density gradient centrifugation was used to separate phage particles from contaminating luciferase protein to reduce background.

Example 4. Bacterial Detection Via Indicator Phage Using Spin Column Filters

FIG. 5 illustrates use of indicator phage and spin column filters for bacterial detection, according to an embodiment of the invention. In an example experiment, E. coli DH10B was grown in Luria-Bertani broth (LB) at 37° C. with shaking. T7SELECT® 415-Luc phage were diluted to 10⁸PFU/40 μL (2.5×10⁹PFU/mL). Cells were counted and diluted to 3000, 300, 30 and 3 cells/mL. A CFU assay was performed in parallel with the following luciferase assay to determine the actual number of input cells per assay.

For each cell dilution, 0.1 mL was added to filters in triplicate. Filters were spun at 600 g for 1 minute. Next, 40 μL of each of the phage dilution was added to each filter, followed by incubation for 10 min at room temperature. Filters were washed twice by addition of 400 PBST (0.05% Tween®), followed by centrifugation at 600 g for 1 minute. Next 50 μL LB was added, followed by incubation for 30 minutes at 37° C. Filters were spun at 6800 g for 2 minutes. Next, 30 μL of the filtrate was transferred to a LUMITRAC® 200 96-well luminometer plate, and a luciferase assay was performed in a Promega® luminometer with injection of 100 μL Luciferase Assay Reagent (Promega, Inc.). Cell count was corrected according to the number of colonies in the parallel CFU assay. The signal to background ratio was obtained by dividing each well's signal by the average of signal from zero cell controls. FIG. 6 shows results demonstrating high sensitivity of the assay for detecting as few as 1 to 3 E. coli cells, via luciferase activity. FIG. 7 shows results demonstrating the very large detection range of the same method using serial dilutions of the starting bacterial sample. This shows detection from an average of 1.4 cells to 14 million cells.

Example 5. Bacterial Detection Via Indicator Phage Using 96-Well Filter Plates

E. coli DH10B was grown in LB at 37° C. with shaking. T7SELECT®415-Luc phage were diluted to 4×10⁷PFU/20 μL in LB (2×10⁹PFU/mL). Cells were counted and diluted to 500, 50 and 5 cells/mL (0.1 mL was added to each wells, giving ˜50, 5 and <1 cells shown in FIG. 5 ). A CFU assay was performed in parallel with the following luciferase assay to determine the actual number of input cells per assay.

For each cell dilution, 0.1 mL was added to multiple wells in a 96-well filter plate: 9 wells for 0.5 cells and 3 wells for 50 cells, 5 cells and the zero cell control. The 96-well filter plate was spun at 1200 rpm (263 rcf) for 3 minutes. Next 20 μL of the phage dilution was added to each filter and incubated for 10 minutes at room temperature, followed by 30 minutes at 37° C. The luciferase assay was performed directly in the original filter plate with 100 μL Luciferase Assay Reagent (Promega, Inc.) injection using a Promega® Luminometer, and plates were read immediately following injection and reread at 15 and 30 minutes thereafter. Cell count was corrected according to the number of colonies in the parallel CFU assay. Signal to background ratios were obtained by dividing each well's signal by the average of signal from zero cell controls.

FIG. 8 shows results demonstrating the use of the 96-well filter plate for detecting single E. coli cells in each well (0.5 cells on average were assayed, such that about one-half of the wells received single cells), and 5.4 and 54 cells per well.

FIG. 9 shows results demonstrating a very large cell detection range, using the 96-well filter plate system, from less than 1 cell per well on average (single cells) to at least 14 million cells per well.

Example 6. Filter Plate Assay Using JG04-NANOLUC® Indicator Phage and Low Cell Concentration

E. coli O157:H7 cells were grown in LB at 37° C. with 220 rpm shaking. JG04-NANOLUC® Indicator Phage were prepared to 10⁶PFU/20 μL. Cells were counted and diluted to 7290, 2430, 810, 270, 90, 30, 10 and 0 cells/mL. Aliquots of 100 μL of each sample were deposited into wells of a PERKINELMER® Optiplate 96-well Grey Luminometer 0.45 μm filter plate in replicates.

As illustrated in FIG. 10 , plates were loaded into a swinging bucket centrifuge and spun at 2400 rpm for 3 minutes. 20 μL of JG04-NANOLUC® phage dilution was added to each well, giving a final concentration of 5×10⁷PFU/mL. Plates were incubated for 10 minutes at room temperature, 200 μL PBST was added to each well, and plates were spun down for 3 minutes at 2400 rpm to wash away excess parental JG04-NANOLUC® phage.

Next, 50 μL LB was added to each well and plates were incubated for 45 minutes in a 37° C. incubator without shaking. Aliquots of 10 μL Promega® Renilla Luciferase Lysis Buffer were added to wells, analyte was transferred to the wells, and luciferase assay was performed with 50 μL Promega® NANOGLO® Reagent injection. Samples with cells were compared to 0 cell controls.

As seen in FIG. 11 , the NANOLUC® Filter Plate results show statistically significant differences between the signal from 0 cells and 1 cell/assay (p value=0.034 by Student's t-Test), demonstrating the ability to detect single cells. More bacterial cells per assay show increasing signal in a dose dependent manner.

Example 7. No Concentration Assay with Low Cell Concentrations

In preparation for an experiment similar to the assay illustrated in schematic FIG. 12 , E. coli O157:H7 cells were grown in LB at 37° C. with 220 rpm shaking. JG04-OpLuc Indicator Phage were prepared to 1.2×10⁷PFU/20 μL, and 20 μL aliquots were distributed to wells of a PERKINELMER® Optiplate 96-well Grey Luminometer plate. Cells were counted and diluted to 10, 3.3, 1.1 and 0 cells/mL. Aliquots of 100 μL of each sample were distributed into wells in replicates (12× for 0.11 and 0.33 cells/assay and 5× for 1 cell/assay), giving a final phage concentration of 10⁸PFU/mL.

Plates were incubated for 45 minutes in a 37° C. incubator without shaking. Finally, 10 μL PROMEGA® Renilla Luciferase Lysis Buffer was added to each well, and the luciferase assay was performed with 50 μL PROMEGA® Renilla Luciferase Assay Reagent (coelenterazine) injection. Samples were compared to 0 cell controls.

As seen in FIG. 13 , the No Concentration Assay with low cell concentration samples results show statistically significant differences between the signal from 0 cells and 1 cell/assay (p value=0.0024 by ANOVA test), demonstrating the ability to detect single cells. Thus the assay is surprisingly sensitive. Samples with fewer than 1 cell per well appear to show a proportional number of wells above the background signal.

Example 8. No Concentration Assay with Wide Cell Concentration Range

In a similar experiment with higher cell concentrations, E. coli O157:H7 cells were grown in LB at 37° C. with 220 rpm shaking. JG04-OpLuc Indicator Phage were prepared to 1.2×10⁷PFU/20 μL, and 20 μL aliquots were distributed to wells of a PERKINELMER® Optiplate 96-well Grey Luminometer plate. Cells were counted and diluted to 10⁸, 10⁷, 10⁶, 10⁵, 10⁴, 10³, 10², 33, 11, 3.7, 1.2 and 0 cells/mL. Aliquots of 100 μL of each sample were distributed into wells in replicates, giving a final phage concentration of 10⁸PFU/mL.

Plates were incubated for 45 minutes in a 37° C. incubator without shaking. 10 μL PROMEGA® Renilla Luciferase Lysis Buffer was added to each well, and luciferase assay was performed with 50 μL PROMEGA® Renilla Luciferase Assay Reagent (coelenterazine) injection. Samples were compared to 0 cell controls.

As seen in FIG. 14 , the experiment for the No Concentration Assay with a very wide range of cell concentration samples shows statistically significant differences between the signal from 0 cells and 1.1 cell/assay (p value=0.000702 by Student's t-Test), demonstrating the ability to detect single cells. More bacterial cells per assay show increasing signal in a dose dependent manner, up to at least 10⁶bacterial cells/mL, surprisingly demonstrating a very wide range of detection.

Example 9. No Concentration Assay with Vegetable Wash Samples

To prepare the vegetable wash, vegetable leaves (e.g., spinach or lettuce) were weighed and added to a clean plastic bag. One mL of LB (+/−0.01-0.05% Tween®20) was added per each gram (g) of vegetable. Leaves and solution were mixed manually for a few minutes. Liquid was then extracted from the plastic bag and used as the “vegetable wash.” Using this method, ˜1 million bacteria were found by CFU to reside on a single spinach leaf (1-2 g).

E. coli O157:H7 cells were grown in LB at 37° C. with 220 rpm shaking. JG04-OpLuc Indicator Phage were prepared to 1.2×10⁷PFU/20 μL, and 20 μL aliquots were distributed to wells of a PERKINELMER® Optiplate 96-well Grey Luminometer plate. Cells were counted and diluted into Vegetable Wash at 120, 60, 30, and 0 cells/mL. Aliquots of 100 μL of each sample were distributed into wells in replicates, giving a final phage concentration of 10⁸PFU/mL.

As seen in FIG. 15 , the experiment for the No Concentration Assay using vegetable wash samples shows marked differences between the signal from 0 cells and 3 cells/assay, demonstrating the ability to detect single-digit cell numbers in vegetable wash. Using more bacterial cells per assay shows increasing signal in a dose dependent manner. The vegetable wash contains about 10⁶non-target bacteria/mL, corresponding to about 10⁵non-target bacteria in this assay (including the 0 cell E. coli O157:H7 control). The ability to discern as few as 3 target bacterial cells from 10⁵non-target bacteria is surprising and again demonstrates the specificity of the assay.

Example 10. Specific and Quantitative Capture of E. coli O157:H7 Using Antibodies and Beads

FIG. 16 depicts an example experiment demonstrating that antibodies against E. coli O157:H7 and magnetic streptavidin-coated beads captured E. coli O157:H7 specifically and quantitatively from samples, but not E. coli B or Salmonella typhimurium in samples. In order to demonstrate specificity in capturing intact, viable bacterial cells from solution, polyclonal antibodies to surface epitopes of E. coli O157:H7 were purchased from KPL (affinity- and reverse-purified to minimize cross-reactivity).

Cultures of both E. coli species and S. typhimurium were grown in LB broth, harvested, and washed with phosphate buffer (1.1 mM KH₂PO₄, 5.6 mM Na₂HPO₄, 154 mM NaCl, pH 7.4). The washed cells were then counted and diluted to a concentration between 5-20 cells per mL.

A sample containing E. coli O157:H7 was combined with a solution containing BSA and biotin-conjugated antibody. Approximately 10 ng biotinylated, polyclonal anti-E. coli antibody (equivalent to about 4×10¹⁰antibody molecules) produced by KPL was added to each of the cell suspensions. A control experiment, where antibody was not added to the cell suspension, was also performed in parallel. The BSA concentration was ˜1%, and the total biotin-antibody was 10 ng. The mixture was rotated end-over-end for 1 hour.

Following incubation with antibodies, 4×10⁷streptavidin-coated magnetic microparticles (Invitrogen®/Life Technologies) were added to the mixture and incubated a further 30 minutes. The cell-antibody-bead complexes were then collected using a magnetic stand, and the unbound fraction (supernatant) was removed. The beads were gently washed with phosphate buffer with Tween® (1.1 mM KH₂PO₄, 5.6 mM Na₂HPO₄, 154 mM NaCl, pH 7.4, 0.05% Tween®). Both the supernatants and captured cell-bead complexes were then spread onto LB agar plates and the plates incubated overnight at 37° C. to determine CFU. Capture of E. coli O157:H7 with anti-O157:H7 antibodies, but not E. coli B or Salmonella typhimurium, was specific and quantitative.

Example 11. Hybrid Immuno-Phage (HIP) Assay

As illustrated in schematic FIG. 17 , the Hybrid Immuno-Phage or “HIP” assay combines the benefits of bacterium-specific antibody capture with the benefits of a modified bacteriophage. The sample is first applied to the microtiter plate well coated with bacterium-specific antibodies (1702). The plate is then centrifuged to facilitate binding of the bacterium to the capture antibodies (1704). Following sufficient time to allow for complete capture of bacteria, a solution containing bacterium-specific Luc-phage is added to each sample (1706). Incubation with the phage results in the binding and attachment of a single or multiple phages to the captured bacterium (1708). Finally, the sample is incubated to facilitate phage replication and luciferase expression, which leads to cell lysis and release of soluble luciferase (1710).

In a HIP assay experiment, a white 96-well ELISA plate was coated with 300 ng monoclonal antibody (in 100 μL PBS) specific to the bacterium of interest at room temperature for 2-3 hours. Wells were washed with PBS (200 μL×3 washes), blocked with 5% BSA/PBS (300 μL) at room temperature for 1-1.5 hours, and again washed with 300 μL PBS×1. Test samples (100 μL) were applied to the wells.

The ELISA plate was centrifuged at 700×g for 30 minutes and then incubated at room temperature for 1 hour. JG04-NANOLUC® phage was added to samples (2-4×10⁶PFU in 10 μL LB) and incubated at room temperature for 10 minutes. Samples were washed with PBS (200 μL×2 washes). LB medium was added to samples (100 μL) and incubated at 37° C. for 1.5 hours.

NANOGLO® substrate (50 μL) was added directly to the samples, and the luminescence was measured in a luminometer. As seen in FIG. 18 , the HIP assay was able to detect 100 and 1,000 E. coli O157:H7 cells in LB medium with approximately 2×10⁶PFU JG04-NANOLUC® phage. The average signal over a no-cell sample is shown on a log scale and ranged from approximately 50-fold for the 100 cell sample to over 1,000-fold for the 1,000 cell sample.

Claims

We claim:

1. A method for detecting a bacterium of interest in a sample, the method comprising the steps of:

incubating at least one bacterium with a plurality of a bacteriophage genetically engineered to have an indicator gene inserted into a late gene region of the bacteriophage, wherein the indicator gene encodes a luciferase protein such that the luciferase protein is expressed during the replication of the bacteriophage and the luciferase protein does not form a fusion protein with a native gene product, and wherein the incubating step is performed at a temperature that is at least 37 degrees Celsius and no greater than 45 degrees Celsius; and

detecting the luciferase protein,

wherein detection of the luciferase protein indicates that the bacterium is present in the sample.

2. The method of claim 1, wherein expression of the luciferase protein is driven by a viral capsid promoter and the luciferase is not incorporated into the structure of the bacteriophage.

3. The method of claim 1, wherein the method is performed without culturing for enrichment of bacteria in the sample.

4. The method of claim 1, wherein the bacteriophage express a luciferase protein.

5. The method of claim 1, wherein the bacteriophage is T4 phage.

6. The method of claim 1, wherein the bacterium is E. coli.

7. The method of claim 1, wherein transcription of the indicator gene is driven by a constitutive bacterial promoter.

8. The method of claim 1, wherein the method further comprises isolating the bacterium from other components in the sample before contacting with the plurality of the bacteriophage.

9. The method of claim 8, wherein the isolating the bacterium comprises binding of the bacterium to a binding agent; or wherein the step of isolating the bacterium comprises contacting the bacterium with a binding agent that is bound to a solid support.

10. The method of claim 9, wherein the binding agent is an antibody specific for the bacterium.

11. The method of claim 8, wherein isolating comprises concentrating the bacterium from the sample on a bacteriological filter.